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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term:benzothiazoles
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Accession:CHEBI:37947 term browser browse the term
Synonyms:xref_mesh: MESH:D052160


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benzothiazoles term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Bax BCL2 associated X, apoptosis regulator increases expression ISO Benzothiazoles metabolite results in increased expression of BAX mRNA CTD PMID:23339777 NCBI chr 1:95,940,001...95,945,407
Ensembl chr 1:95,938,808...95,945,368 		JBrowse link
G Bcl2 BCL2, apoptosis regulator decreases expression ISO Benzothiazoles metabolite results in decreased expression of BCL2 mRNA CTD PMID:23339777 NCBI chr13:22,689,783...22,853,920
Ensembl chr13:22,684,989...22,853,743
Ensembl chr13:22,684,989...22,853,743 		JBrowse link
G Bcl2l1 Bcl2-like 1 decreases expression ISO Benzothiazoles metabolite results in decreased expression of BCL2L1 mRNA CTD PMID:23339777 NCBI chr 3:141,253,508...141,304,582
Ensembl chr 3:141,253,523...141,303,479
Ensembl chr 1:141,253,523...141,303,479 		JBrowse link
(4-oxo-3-\{[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl\}-3,4-dihydrophthalazin-1-yl)acetic acid term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Akr1b1 aldo-keto reductase family 1 member B1 decreases activity
multiple interactions		 ISO zopolrestat results in decreased activity of AKR1B1 protein
[zopolrestat results in decreased activity of AKR1B1 protein] inhibits the reaction [Antigens, Plant results in increased abundance of Reactive Oxygen Species]; [zopolrestat results in decreased activity of AKR1B1 protein] inhibits the reaction [Antigens, Plant results in increased secretion of Dinoprostone]; [zopolrestat results in decreased activity of AKR1B1 protein] which results in decreased susceptibility to Antigens, Plant		 CTD PMID:21334316 NCBI chr 4:62,932,033...62,946,126
Ensembl chr 4:62,932,031...62,946,157 		JBrowse link
G Akr1b10 aldo-keto reductase family 1 member B10 multiple interactions
decreases activity		 ISO zopolrestat inhibits the reaction [AKR1B10 protein results in increased reduction of Daunorubicin]; zopolrestat inhibits the reaction [AKR1B10 protein results in increased reduction of Glyceraldehyde]
zopolrestat results in decreased activity of AKR1B10 protein; zopolrestat results in decreased activity of AKR1B10 protein mutant form		 CTD PMID:18325492 PMID:19028477 NCBI chr 4:63,038,459...63,060,336
Ensembl chr 4:63,040,169...63,053,852 		JBrowse link
G Ccl4 C-C motif chemokine ligand 4 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of CCL4 mRNA] CTD PMID:21334316 NCBI chr10:68,466,394...68,468,229
Ensembl chr10:68,452,052...68,468,231 		JBrowse link
G Ccl5 C-C motif chemokine ligand 5 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of CCL5 mRNA] CTD PMID:21334316 NCBI chr10:68,322,826...68,327,380
Ensembl chr10:68,322,829...68,327,377 		JBrowse link
G Il10 interleukin 10 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL10 mRNA] CTD PMID:21334316 NCBI chr13:42,472,625...42,477,308
Ensembl chr13:42,472,839...42,477,313 		JBrowse link
G Il13 interleukin 13 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL13 mRNA] CTD PMID:21334316 NCBI chr10:37,790,130...37,792,687
Ensembl chr10:37,790,130...37,792,737 		JBrowse link
G Il18 interleukin 18 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL18 mRNA] CTD PMID:21334316 NCBI chr 8:50,904,630...50,932,887
Ensembl chr 8:50,906,960...50,932,887 		JBrowse link
G Il4 interleukin 4 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL4 mRNA] CTD PMID:21334316 NCBI chr10:37,771,203...37,776,750
Ensembl chr10:37,771,203...37,776,750 		JBrowse link
G Il5 interleukin 5 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL5 mRNA] CTD PMID:21334316 NCBI chr10:37,874,342...37,877,213
Ensembl chr10:37,874,342...37,877,213 		JBrowse link
G Il6 interleukin 6 multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of IL6 mRNA]
zopolrestat inhibits the reaction [Antigens, Plant results in increased secretion of IL6 protein]		 CTD PMID:21334316 NCBI chr 4:5,214,602...5,219,178
Ensembl chr 4:5,213,394...5,219,178 		JBrowse link
G Jak2 Janus kinase 2 multiple interactions EXP zopolrestat results in decreased phosphorylation of and results in decreased activity of JAK2 protein CTD PMID:15746188 NCBI chr 1:226,995,334...227,054,381
Ensembl chr 1:226,995,334...227,054,189 		JBrowse link
G Nos2 nitric oxide synthase 2 multiple interactions ISO zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased expression of NOS2 mRNA]; zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased expression of NOS2 protein] CTD PMID:24021941 NCBI chr10:63,815,308...63,851,208
Ensembl chr10:63,815,308...63,851,210 		JBrowse link
G Ptgs2 prostaglandin-endoperoxide synthase 2 multiple interactions ISO zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased expression of PTGS2 mRNA]; zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased expression of PTGS2 protein] CTD PMID:24021941 NCBI chr13:62,163,936...62,172,193
Ensembl chr13:62,163,932...62,172,188 		JBrowse link
G Rela RELA proto-oncogene, NF-kB subunit multiple interactions ISO zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 affects the localization of RELA protein]; zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased phosphorylation of RELA protein] CTD PMID:24021941 NCBI chr 1:202,925,001...202,935,484
Ensembl chr 1:202,924,945...202,935,484 		JBrowse link
G Stat5a signal transducer and activator of transcription 5A multiple interactions EXP zopolrestat results in decreased phosphorylation of and results in decreased activity of STAT5A protein CTD PMID:15746188 NCBI chr10:85,785,537...85,809,869
Ensembl chr10:85,785,537...85,809,866 		JBrowse link
G Tnf tumor necrosis factor multiple interactions ISO zopolrestat inhibits the reaction [Antigens, Plant results in increased expression of TNF mRNA]; zopolrestat inhibits the reaction [lipopolysaccharide, E coli O55-B5 results in increased expression of TNF protein] CTD PMID:21334316 PMID:24021941 NCBI chr20:3,622,011...3,624,629
Ensembl chr20:3,622,011...3,624,629 		JBrowse link
1,3-benzothiazole-2-thiol term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ahr aryl hydrocarbon receptor increases expression ISO captax results in increased expression of AHR mRNA CTD PMID:21590714 NCBI chr 6:52,234,089...52,271,568
Ensembl chr 6:52,234,089...52,271,568 		JBrowse link
G Akr1c2 aldo-keto reductase family 1, member C2 increases activity
increases expression		 ISO captax results in increased activity of AKR1C2 promoter
captax results in increased expression of AKR1C2 mRNA		 CTD PMID:20491607 PMID:20713136 PMID:21195160 NCBI chr17:65,759,778...65,808,013
Ensembl chr17:65,759,788...65,775,764 		JBrowse link
G Ampd3 adenosine monophosphate deaminase 3 increases expression ISO captax results in increased expression of AMPD3 mRNA CTD PMID:24211530 NCBI chr 1:164,884,823...164,929,899
Ensembl chr 1:164,885,320...164,929,887 		JBrowse link
G Atf3 activating transcription factor 3 increases expression ISO captax results in increased expression of ATF3 mRNA CTD PMID:23999411 NCBI chr13:102,751,278...102,800,520
Ensembl chr13:102,751,321...102,764,631 		JBrowse link
G Ccl2 C-C motif chemokine ligand 2 decreases expression ISO captax results in decreased expression of CCL2 mRNA CTD PMID:20713136 NCBI chr10:67,005,424...67,007,222
Ensembl chr10:67,005,424...67,007,226 		JBrowse link
G Ccl4 C-C motif chemokine ligand 4 increases secretion ISO captax results in increased secretion of CCL4 protein CTD PMID:16314067 NCBI chr10:68,466,394...68,468,229
Ensembl chr10:68,452,052...68,468,231 		JBrowse link
G Ccr2 C-C motif chemokine receptor 2 increases expression ISO captax results in increased expression of CCR2 mRNA CTD PMID:20713136 NCBI chr 8:123,734,465...123,742,483
Ensembl chr 8:123,734,430...123,742,100 		JBrowse link
G Ccr5 C-C motif chemokine receptor 5 increases expression ISO captax results in increased expression of CCR5 mRNA CTD PMID:20713136 NCBI chr 8:123,752,423...123,757,538
Ensembl chr 8:123,752,325...123,759,260 		JBrowse link
G Cd86 CD86 molecule increases expression ISO captax results in increased expression of CD86 protein CTD PMID:12423654 NCBI chr11:64,142,193...64,200,816
Ensembl chr11:64,163,828...64,200,818 		JBrowse link
G Creb1 cAMP responsive element binding protein 1 decreases expression ISO captax results in decreased expression of CREB1 mRNA CTD PMID:20385217 NCBI chr 9:65,903,511...65,972,562
Ensembl chr 9:65,903,547...65,970,816 		JBrowse link
G Cxcl1 C-X-C motif chemokine ligand 1 increases expression ISO captax results in increased expression of CXCL1 mRNA CTD PMID:20713136 NCBI chr14:17,193,364...17,195,143
Ensembl chr14:17,193,365...17,195,215 		JBrowse link
G Cxcl14 C-X-C motif chemokine ligand 14 decreases expression ISO captax results in decreased expression of CXCL14 mRNA; captax results in decreased expression of CXCL14 protein CTD PMID:31734321 NCBI chr17:8,317,930...8,325,956
Ensembl chr17:8,317,933...8,324,839 		JBrowse link
G Cxcl2 C-X-C motif chemokine ligand 2 increases expression ISO captax results in increased expression of CXCL2 protein CTD PMID:23178550 NCBI chr14:17,181,030...17,183,075
Ensembl chr14:17,181,062...17,183,075 		JBrowse link
G Cxcl3 C-X-C motif chemokine ligand 3 increases expression ISO captax results in increased expression of CXCL1 mRNA CTD PMID:20713136 NCBI chr14:17,287,727...17,289,451
Ensembl chr14:17,270,146...17,289,511 		JBrowse link
G Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 increases expression ISO captax results in increased expression of CYP1A1 mRNA CTD PMID:20491607 NCBI chr 8:58,096,021...58,102,130
Ensembl chr 8:58,096,077...58,102,125 		JBrowse link
G Dio1 iodothyronine deiodinase 1 decreases activity ISO captax results in decreased activity of DIO1 protein CTD PMID:29228274 NCBI chr 5:122,074,285...122,090,983
Ensembl chr 5:122,074,279...122,090,970 		JBrowse link
G Dnajb4 DnaJ heat shock protein family (Hsp40) member B4 increases expression ISO captax results in increased expression of DNAJB4 mRNA CTD PMID:23999411 PMID:27965148 NCBI chr 2:241,129,346...241,159,272
Ensembl chr 2:241,130,340...241,159,089 		JBrowse link
G Enpp2 ectonucleotide pyrophosphatase/phosphodiesterase 2 increases expression ISO captax results in increased expression of ENPP2 protein CTD PMID:22952646 NCBI chr 7:86,202,345...86,325,050
Ensembl chr 7:86,202,350...86,324,827 		JBrowse link
G F3 coagulation factor III, tissue factor increases expression ISO captax results in increased expression of F3 protein CTD PMID:25569083 NCBI chr 2:209,827,061...209,838,666
Ensembl chr 2:209,826,959...209,838,668 		JBrowse link
G Fth1 ferritin heavy chain 1 increases expression ISO captax results in increased expression of FTH1 mRNA CTD PMID:24211530 NCBI chr 1:206,627,142...206,629,430
Ensembl chr 1:206,627,103...206,725,424 		JBrowse link
G Ftl1 ferritin light chain 1 increases expression ISO captax results in increased expression of FTL mRNA CTD PMID:24211530 NCBI chr 1:95,936,387...95,938,234
Ensembl chr 1:95,936,387...95,939,725
Ensembl chr10:95,936,387...95,939,725
Ensembl chr 2:95,936,387...95,939,725 		JBrowse link
G Gclc glutamate-cysteine ligase, catalytic subunit increases expression ISO captax results in increased expression of GCLC mRNA CTD PMID:20491607 NCBI chr 8:78,629,899...78,668,547
Ensembl chr 8:78,630,127...78,668,544 		JBrowse link
G Gclm glutamate cysteine ligase, modifier subunit increases expression ISO captax results in increased expression of GCLM mRNA CTD PMID:23999411 PMID:24211530 NCBI chr 2:210,347,482...210,367,537
Ensembl chr 2:210,347,482...210,367,535 		JBrowse link
G H2ax H2A.X variant histone increases expression
multiple interactions		 ISO captax results in increased expression of H2AX protein
1-aminobenzotriazole inhibits the reaction [captax results in increased expression of H2AX protein]; 2-morpholin-4-yl-6-thianthren-1-yl-pyran-4-one inhibits the reaction [captax results in increased expression of H2AX protein]; Acetylcysteine inhibits the reaction [captax results in increased expression of H2AX protein]; Disulfiram inhibits the reaction [captax results in increased expression of H2AX protein]		 CTD PMID:35279910 NCBI chr 8:44,671,907...44,673,262
Ensembl chr 8:44,671,786...44,673,239
Ensembl chr 4:44,671,786...44,673,239 		JBrowse link
G Hmox1 heme oxygenase 1 increases expression ISO captax results in increased expression of HMOX1 mRNA CTD PMID:20713136 PMID:23445166 PMID:24211530 NCBI chr19:13,466,287...13,474,082
Ensembl chr19:13,467,244...13,474,079 		JBrowse link
G Hspa6l-ps1 heat shock protein family A (Hsp70) member 6 like, pseudogene 1 increases expression ISO captax results in increased expression of HSPA6 mRNA CTD PMID:23999411 NCBI chr13:83,273,176...83,274,317 JBrowse link
G Ifng interferon gamma increases secretion ISO captax results in increased secretion of IFNG protein CTD PMID:22245253 NCBI chr 7:53,903,339...53,907,375
Ensembl chr 7:53,903,337...53,907,375 		JBrowse link
G Il18 interleukin 18 increases expression ISO captax results in increased expression of IL18 protein CTD PMID:23063874 NCBI chr 8:50,904,630...50,932,887
Ensembl chr 8:50,906,960...50,932,887 		JBrowse link
G Il1a interleukin 1 alpha increases expression ISO captax results in increased expression of IL1A protein
captax results in increased expression of IL1A mRNA		 CTD PMID:23178550 PMID:33715048 NCBI chr 3:116,526,601...116,537,055
Ensembl chr 3:116,526,604...116,536,822 		JBrowse link
G Il1b interleukin 1 beta increases expression
increases secretion		 ISO captax results in increased expression of IL1B mRNA
captax results in increased secretion of IL1B protein		 CTD PMID:33715048 NCBI chr 3:116,577,005...116,583,386
Ensembl chr 3:116,577,010...116,583,415 		JBrowse link
G Il2 interleukin 2 increases secretion ISO captax results in increased secretion of IL2 protein CTD PMID:22245253 NCBI chr 2:120,004,862...120,009,566
Ensembl chr 2:120,004,862...120,009,566 		JBrowse link
G Il6 interleukin 6 increases secretion ISO captax results in increased secretion of IL6 protein CTD PMID:22245253 NCBI chr 4:5,214,602...5,219,178
Ensembl chr 4:5,213,394...5,219,178 		JBrowse link
G Il7r interleukin 7 receptor increases expression ISO captax results in increased expression of IL7R mRNA CTD PMID:20713136 NCBI chr 2:58,452,393...58,477,757
Ensembl chr 2:58,454,217...58,477,757 		JBrowse link
G Mir146a microRNA 146a increases expression ISO captax results in increased expression of MIR146A mRNA CTD PMID:37326882 NCBI chr10:27,848,516...27,848,610
Ensembl chr10:27,848,516...27,848,610 		JBrowse link
G Mmp9 matrix metallopeptidase 9 increases expression ISO captax results in increased expression of MMP9 mRNA; captax results in increased expression of MMP9 protein CTD PMID:22952646 NCBI chr 3:153,684,158...153,692,118
Ensembl chr 3:153,683,858...153,692,120 		JBrowse link
G Myc MYC proto-oncogene, bHLH transcription factor increases expression ISO captax results in increased expression of MYC mRNA CTD PMID:24211530 NCBI chr 7:93,593,705...93,598,633
Ensembl chr 7:93,593,705...93,598,630 		JBrowse link
G Nfkb1 nuclear factor kappa B subunit 1 affects expression ISO captax affects the expression of NFKB1 mRNA CTD PMID:20385217 NCBI chr 2:224,016,214...224,132,135
Ensembl chr 2:224,016,214...224,110,404 		JBrowse link
G Notch3 notch receptor 3 decreases expression ISO captax results in decreased expression of NOTCH3 mRNA CTD PMID:20713136 NCBI chr 7:11,132,984...11,184,025
Ensembl chr 7:11,133,706...11,184,025 		JBrowse link
G Nqo1 NAD(P)H quinone dehydrogenase 1 increases expression ISO captax results in increased expression of NQO1 mRNA CTD PMID:24211530 NCBI chr19:35,295,633...35,310,528
Ensembl chr19:35,295,573...35,310,557 		JBrowse link
G Pmaip1 phorbol-12-myristate-13-acetate-induced protein 1 increases expression ISO captax results in increased expression of PMAIP1 mRNA CTD PMID:20713136 NCBI chr18:59,986,020...59,992,434
Ensembl chr18:59,986,017...59,992,429 		JBrowse link
G Rgs1 regulator of G-protein signaling 1 increases expression ISO captax results in increased expression of RGS1 mRNA CTD PMID:20713136 NCBI chr13:56,018,546...56,022,889
Ensembl chr13:56,018,554...56,022,984 		JBrowse link
G Sel1l3 SEL1L family member 3 increases expression ISO captax results in increased expression of SEL1L3 mRNA CTD PMID:24211530 NCBI chr14:57,775,515...57,882,076
Ensembl chr14:57,775,501...57,882,644 		JBrowse link
G Slc5a5 solute carrier family 5 member 5 multiple interactions ISO captax inhibits the reaction [SLC5A5 protein results in increased uptake of Iodine] CTD PMID:27979590 NCBI chr16:18,546,709...18,556,698
Ensembl chr16:18,546,709...18,556,697 		JBrowse link
G Slc7a11 solute carrier family 7 member 11 increases expression ISO captax results in increased expression of SLC7A11 mRNA CTD PMID:24211530 NCBI chr 2:134,382,002...134,517,622
Ensembl chr 2:133,963,107...134,517,536 		JBrowse link
G Sqstm1 sequestosome 1 increases expression ISO captax results in increased expression of SQSTM1 mRNA CTD PMID:24211530 NCBI chr10:34,525,517...34,536,670
Ensembl chr10:34,525,519...34,536,673 		JBrowse link
G Syne2 spectrin repeat containing nuclear envelope protein 2 decreases expression ISO captax results in decreased expression of SYNE2 mRNA CTD PMID:24211530 NCBI chr 6:94,537,088...94,848,085
Ensembl chr 6:94,537,088...94,848,064 		JBrowse link
G Tnf tumor necrosis factor decreases expression ISO captax results in decreased expression of TNF mRNA CTD PMID:20385217 NCBI chr20:3,622,011...3,624,629
Ensembl chr20:3,622,011...3,624,629 		JBrowse link
G Tnnt2 troponin T2, cardiac type decreases expression ISO captax results in decreased expression of TNNT2 mRNA CTD PMID:24211530 NCBI chr13:47,267,325...47,285,390
Ensembl chr13:47,267,204...47,285,388 		JBrowse link
G Tpo thyroid peroxidase multiple interactions
decreases activity		 ISO
EXP		 captax binds to and results in decreased activity of TPO protein
captax results in decreased activity of TPO protein		 CTD PMID:23959146 PMID:26865668 PMID:26884060 PMID:31629072 NCBI chr 6:46,698,402...46,768,199
Ensembl chr 6:46,698,414...46,768,199 		JBrowse link
G Txnrd1 thioredoxin reductase 1 increases expression ISO captax results in increased expression of TXNRD1 mRNA CTD PMID:23445166 PMID:24211530 NCBI chr 7:20,830,042...20,914,990
Ensembl chr 7:20,830,045...20,907,863 		JBrowse link
G Vegfa vascular endothelial growth factor A increases expression ISO captax results in increased expression of VEGFA protein CTD PMID:25617811 NCBI chr 9:14,955,300...14,970,641
Ensembl chr 9:14,955,300...14,970,641 		JBrowse link
benzothiazole term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ahr aryl hydrocarbon receptor affects binding ISO benzothiazole binds to AHR protein; benzothiazole metabolite binds to AHR protein CTD PMID:16705413 NCBI chr 6:52,234,089...52,271,568
Ensembl chr 6:52,234,089...52,271,568 		JBrowse link
G Ephx1 epoxide hydrolase 1 increases expression EXP benzothiazole results in increased expression of EPHX1 mRNA CTD PMID:8951341 NCBI chr13:92,714,315...92,744,105
Ensembl chr13:92,714,315...92,790,235 		JBrowse link
G Gsta2 glutathione S-transferase alpha 2 increases expression EXP benzothiazole results in increased expression of GSTA2 mRNA CTD PMID:8951341 NCBI chr 8:79,184,535...79,196,827
Ensembl chr 8:79,184,322...79,196,798 		JBrowse link
G Gstm1 glutathione S-transferase mu 1 increases expression EXP benzothiazole results in increased expression of GSTM1 mRNA CTD PMID:8951341 NCBI chr 2:195,649,845...195,655,402
Ensembl chr 2:195,649,845...195,655,411 		JBrowse link
G Gstm2 glutathione S-transferase mu 2 increases expression EXP benzothiazole results in increased expression of GSTM2 mRNA CTD PMID:8951341 NCBI chr 2:195,624,015...195,628,774
Ensembl chr 2:195,544,426...195,628,961 		JBrowse link
C3-thiacarbocyanine cation term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Kcnh2 potassium voltage-gated channel subfamily H member 2 decreases activity ISO Dithiazanine results in decreased activity of KCNH2 protein CTD PMID:28551711 NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008 		JBrowse link
dibenzothiazol-2-yl disulfide term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ifng interferon gamma multiple interactions ISO [dibenzothiazyl disulfide co-treated with Sodium Dodecyl Sulfate] results in increased expression of IFNG protein CTD PMID:12062936 NCBI chr 7:53,903,339...53,907,375
Ensembl chr 7:53,903,337...53,907,375 		JBrowse link
G Il4 interleukin 4 multiple interactions ISO [dibenzothiazyl disulfide co-treated with Sodium Dodecyl Sulfate] results in increased expression of IL4 protein CTD PMID:12062936 NCBI chr10:37,771,203...37,776,750
Ensembl chr10:37,771,203...37,776,750 		JBrowse link
dithiazanine term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Kcnh2 potassium voltage-gated channel subfamily H member 2 decreases activity ISO Dithiazanine results in decreased activity of KCNH2 protein CTD PMID:28551711 NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008 		JBrowse link
E3040 term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Abcc2 ATP binding cassette subfamily C member 2 multiple interactions ISO [SLCO1B1 protein co-treated with ABCC2 protein] results in increased transport of E 3040 analog CTD PMID:19628752 NCBI chr 1:242,664,657...242,723,239
Ensembl chr 1:242,664,657...242,723,238 		JBrowse link
G Abcg2 ATP binding cassette subfamily G member 2 affects export ISO ABCG2 protein affects the export of E 3040 analog CTD PMID:15598971 NCBI chr 4:87,676,241...87,802,757
Ensembl chr 4:87,745,319...87,802,409 		JBrowse link
G Slc22a12 solute carrier family 22 member 12 multiple interactions ISO E 3040 inhibits the reaction [SLC22A12 protein results in increased uptake of Uric Acid] CTD PMID:21272127 NCBI chr 1:203,845,039...203,852,496
Ensembl chr 1:203,845,048...203,853,555 		JBrowse link
ethoxzolamide term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Car1 carbonic anhydrase 1 multiple interactions ISO Ethoxzolamide binds to and results in decreased activity of CA1 protein CTD PMID:17826101 NCBI chr 2:86,829,436...86,872,209
Ensembl chr 2:86,861,897...86,872,208 		JBrowse link
G Car2 carbonic anhydrase 2 multiple interactions ISO Ethoxzolamide binds to and results in decreased activity of CA2 protein CTD PMID:17826101 NCBI chr 2:86,741,625...86,756,766
Ensembl chr 2:86,741,626...86,756,818 		JBrowse link
G Car3 carbonic anhydrase 3 multiple interactions ISO Ethoxzolamide binds to and results in decreased activity of CA3 protein CTD PMID:17826101 NCBI chr 2:86,770,418...86,780,011
Ensembl chr 2:86,770,420...86,784,280 		JBrowse link
lubeluzole term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Kcnh2 potassium voltage-gated channel subfamily H member 2 multiple interactions ISO lubeluzole binds to and results in decreased activity of KCNH2 protein CTD PMID:29550817 NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008 		JBrowse link
mefenacet term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ar androgen receptor multiple interactions ISO Dihydrotestosterone inhibits the reaction [mefenacet results in increased activity of AR protein] CTD PMID:15064155 NCBI chr  X:63,104,771...63,273,934
Ensembl chr  X:63,104,771...63,273,925 		JBrowse link
G Cyp2b3 cytochrome P450, family 2, subfamily b, polypeptide 3 multiple interactions ISO CYP2B6 protein results in increased metabolism of and results in decreased susceptibility to mefenacet CTD PMID:15853388 NCBI chr 1:81,652,762...81,732,153
Ensembl chr 1:81,652,787...81,732,143 		JBrowse link
G Nr1i2 nuclear receptor subfamily 1, group I, member 2 multiple interactions ISO mefenacet binds to and results in increased activity of NR1I2 protein CTD PMID:21115097 NCBI chr11:62,460,213...62,496,665
Ensembl chr11:62,460,213...62,496,658 		JBrowse link
pramipexole term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ache acetylcholinesterase multiple interactions EXP Pramipexole inhibits the reaction [amyloid beta-protein (1-42) results in increased activity of ACHE protein] CTD PMID:35868426 NCBI chr12:19,406,133...19,413,713
Ensembl chr12:19,407,360...19,413,651 		JBrowse link
G Atp5f1a ATP synthase F1 subunit alpha multiple interactions EXP Pramipexole inhibits the reaction [amyloid beta-protein (1-42) results in decreased expression of ATP5F1A protein] CTD PMID:35868426 NCBI chr18:71,292,406...71,300,342
Ensembl chr18:71,292,374...71,300,794 		JBrowse link
G Casp3 caspase 3 multiple interactions EXP pramipexole inhibits the reaction [Hydrogen Peroxide results in increased activity of CASP3 protein] CTD PMID:16362428 NCBI chr16:45,662,910...45,681,171
Ensembl chr16:45,662,910...45,684,648 		JBrowse link
G Drd2 dopamine receptor D2 multiple interactions EXP
ISO		 pramipexole binds to and results in increased activity of DRD2 protein CTD PMID:10728880 NCBI chr 8:49,708,927...49,772,876
Ensembl chr 8:49,708,927...49,772,875 		JBrowse link
G Drd3 dopamine receptor D3 multiple interactions ISO pramipexole binds to and results in increased activity of DRD3 protein CTD PMID:10728880 NCBI chr11:56,879,689...56,931,901
Ensembl chr11:56,879,689...56,940,596 		JBrowse link
G Mapk8 mitogen-activated protein kinase 8 multiple interactions EXP pramipexole inhibits the reaction [Hydrogen Peroxide results in increased phosphorylation of MAPK8 protein] CTD PMID:16362428 NCBI chr16:8,638,897...8,721,960
Ensembl chr16:8,638,924...8,721,981 		JBrowse link
G Mapk9 mitogen-activated protein kinase 9 multiple interactions EXP pramipexole inhibits the reaction [Hydrogen Peroxide results in increased phosphorylation of MAPK9 protein] CTD PMID:16362428 NCBI chr10:34,169,661...34,211,138
Ensembl chr10:34,169,675...34,210,178 		JBrowse link
G Ppargc1a PPARG coactivator 1 alpha increases expression EXP Pramipexole results in increased expression of PPARGC1A protein CTD PMID:35868426 NCBI chr14:58,860,752...59,516,525
Ensembl chr14:58,861,144...59,512,656 		JBrowse link
G Ptprd protein tyrosine phosphatase, receptor type, D increases expression EXP [Pramipexole cotreated with exercise] increases expression of Ptprd protein in the striatum RGD PMID:37633178 RGD:401976430 NCBI chr 5:90,046,993...90,698,977
NCBI chr 5:91,122,354...91,641,754
Ensembl chr 5:90,048,966...92,369,396 		JBrowse link
G Sdhb succinate dehydrogenase complex iron sulfur subunit B multiple interactions EXP Pramipexole inhibits the reaction [amyloid beta-protein (1-42) results in decreased expression of SDHB protein] CTD PMID:35868426 NCBI chr 5:153,264,906...153,285,570
Ensembl chr 5:153,264,899...153,314,293 		JBrowse link
Riluzole term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ar androgen receptor multiple interactions ISO Chloroquine inhibits the reaction [Riluzole results in increased degradation of and results in decreased expression of AR protein alternative form]; Chloroquine inhibits the reaction [Riluzole results in increased degradation of and results in decreased expression of AR protein]; Riluzole promotes the reaction [AR protein binds to SQSTM1 protein]; Riluzole results in increased degradation of and results in decreased expression of AR protein; Riluzole results in increased degradation of and results in decreased expression of AR protein alternative form; Riluzole results in increased degradation of and results in decreased expression of AR protein mutant form; STF 083010 inhibits the reaction [Riluzole results in increased degradation of and results in decreased expression of AR protein] CTD PMID:30280407 NCBI chr  X:63,104,771...63,273,934
Ensembl chr  X:63,104,771...63,273,925 		JBrowse link
G Atf6 activating transcription factor 6 increases expression ISO Riluzole results in increased expression of ATF6 protein CTD PMID:30280407 NCBI chr13:82,927,579...83,106,381
Ensembl chr13:82,930,034...83,107,177 		JBrowse link
G Bcl2 BCL2, apoptosis regulator increases expression EXP Riluzole results in increased expression of BCL2 protein CTD PMID:20885006 NCBI chr13:22,689,783...22,853,920
Ensembl chr13:22,684,989...22,853,743
Ensembl chr13:22,684,989...22,853,743 		JBrowse link
G Casp3 caspase 3 multiple interactions
increases activity		 ISO Palmitic Acid promotes the reaction [Riluzole results in increased activity of CASP3 protein] CTD PMID:19528481 PMID:22700542 NCBI chr16:45,662,910...45,681,171
Ensembl chr16:45,662,910...45,684,648 		JBrowse link
G Casp4 caspase 4 increases activity ISO Riluzole results in increased activity of CASP4 protein CTD PMID:19528481 NCBI chr 8:2,599,017...2,635,097
Ensembl chr 8:2,598,876...2,635,092 		JBrowse link
G Casp7 caspase 7 multiple interactions
increases activity		 ISO Palmitic Acid promotes the reaction [Riluzole results in increased activity of CASP7 protein] CTD PMID:22700542 NCBI chr 1:255,437,438...255,476,737
Ensembl chr 1:255,437,172...255,476,729 		JBrowse link
G Casp8 caspase 8 increases activity ISO Riluzole results in increased activity of CASP8 protein CTD PMID:19528481 NCBI chr 9:60,263,863...60,312,542
Ensembl chr 9:60,264,075...60,312,542 		JBrowse link
G Casp9 caspase 9 increases activity ISO Riluzole results in increased activity of CASP9 protein CTD PMID:19528481 NCBI chr 5:154,108,872...154,126,628
Ensembl chr 5:154,109,046...154,126,626 		JBrowse link
G Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 decreases activity ISO Riluzole results in decreased activity of CYP1A1 protein CTD PMID:33814510 NCBI chr 8:58,096,021...58,102,130
Ensembl chr 8:58,096,077...58,102,125 		JBrowse link
G Cyp1b1 cytochrome P450, family 1, subfamily b, polypeptide 1 decreases activity ISO Riluzole results in decreased activity of CYP1B1 protein CTD PMID:33814510 NCBI chr 6:15,342,312...15,350,886
Ensembl chr 6:15,342,344...15,350,917 		JBrowse link
G Glul glutamate-ammonia ligase multiple interactions EXP Riluzole inhibits the reaction [manganese chloride results in decreased expression of and results in decreased activity of GLUL protein]; Riluzole inhibits the reaction [manganese chloride results in decreased expression of GLUL mRNA] CTD PMID:19615351 NCBI chr13:65,969,053...66,035,121
Ensembl chr13:66,025,630...66,035,108 		JBrowse link
G Hspa5 heat shock protein family A (Hsp70) member 5 increases expression ISO Riluzole results in increased expression of HSPA5 protein CTD PMID:30280407 NCBI chr 3:18,055,507...18,059,969
Ensembl chr 3:18,055,405...18,059,891 		JBrowse link
G Il1a interleukin 1 alpha multiple interactions ISO [IL6 protein co-treated with IL1A protein co-treated with TNF protein co-treated with lipopolysaccharide, Escherichia coli O111 B4] results in increased susceptibility to Riluzole CTD PMID:19362101 NCBI chr 3:116,526,601...116,537,055
Ensembl chr 3:116,526,604...116,536,822 		JBrowse link
G Il6 interleukin 6 multiple interactions ISO [IL6 protein co-treated with IL1A protein co-treated with TNF protein co-treated with lipopolysaccharide, Escherichia coli O111 B4] results in increased susceptibility to Riluzole CTD PMID:19362101 NCBI chr 4:5,214,602...5,219,178
Ensembl chr 4:5,213,394...5,219,178 		JBrowse link
G Jun Jun proto-oncogene, AP-1 transcription factor subunit decreases phosphorylation EXP Riluzole results in decreased phosphorylation of JUN protein CTD PMID:10067977 NCBI chr 5:109,894,175...109,897,268
Ensembl chr 5:109,893,145...109,897,656 		JBrowse link
G Klk1c10 kallikrein 1-related peptidase C10 decreases expression ISO Riluzole results in decreased expression of KLK3 mRNA CTD PMID:30280407 NCBI chr 1:94,402,993...94,407,052
Ensembl chr 1:94,402,993...94,407,052 		JBrowse link
G Nefh neurofilament heavy chain decreases phosphorylation EXP Riluzole results in decreased phosphorylation of NEFH protein CTD PMID:19429076 NCBI chr14:79,830,362...79,840,347
Ensembl chr14:79,830,362...79,840,351 		JBrowse link
G Nefm neurofilament medium chain affects localization
decreases phosphorylation		 EXP Riluzole affects the localization of NEFM protein
Riluzole results in decreased phosphorylation of NEFM protein		 CTD PMID:19429076 NCBI chr15:42,360,449...42,365,753
Ensembl chr15:42,360,454...42,365,755 		JBrowse link
G Nr1i2 nuclear receptor subfamily 1, group I, member 2 increases activity ISO Riluzole results in increased activity of NR1I2 protein CTD PMID:25455453 NCBI chr11:62,460,213...62,496,665
Ensembl chr11:62,460,213...62,496,658 		JBrowse link
G Prkcb protein kinase C, beta multiple interactions ISO Riluzole inhibits the reaction [VEGFA protein results in increased phosphorylation of PRKCB protein] CTD PMID:16303979 NCBI chr 1:176,832,173...177,163,539
Ensembl chr 1:176,832,226...177,163,536 		JBrowse link
G Slc17a7 solute carrier family 17 member 7 decreases expression EXP Riluzole results in decreased expression of SLC17A7 protein CTD PMID:17507170 NCBI chr 1:95,649,709...95,661,591
Ensembl chr 1:95,649,745...95,661,588 		JBrowse link
G Slc1a2 solute carrier family 1 member 2 multiple interactions
increases expression		 EXP Riluzole inhibits the reaction [manganese chloride results in decreased expression of SLC1A2 mRNA]; Riluzole inhibits the reaction [manganese chloride results in decreased expression of SLC1A2 protein]; Riluzole inhibits the reaction [methylmercuric chloride results in decreased expression of and results in decreased activity of SLC1A2 protein]; Riluzole inhibits the reaction [methylmercuric chloride results in decreased expression of SLC1A2 mRNA]
Riluzole results in increased expression of SLC1A2 mRNA; Riluzole results in increased expression of SLC1A2 protein		 CTD PMID:19615351 PMID:22966415 NCBI chr 3:89,005,129...89,135,469
Ensembl chr 3:89,005,129...89,126,498 		JBrowse link
G Slc1a3 solute carrier family 1 member 3 multiple interactions
increases expression		 EXP Riluzole inhibits the reaction [manganese chloride results in decreased expression of SLC1A3 mRNA]; Riluzole inhibits the reaction [manganese chloride results in decreased expression of SLC1A3 protein]; Riluzole inhibits the reaction [methylmercuric chloride results in decreased expression of and results in decreased activity of SLC1A3 protein]; Riluzole inhibits the reaction [methylmercuric chloride results in decreased expression of SLC1A3 mRNA]
Riluzole results in increased expression of SLC1A3 mRNA; Riluzole results in increased expression of SLC1A3 protein		 CTD PMID:19615351 PMID:22966415 NCBI chr 2:57,755,495...57,830,605
Ensembl chr 2:57,755,497...57,830,605 		JBrowse link
G Sqstm1 sequestosome 1 multiple interactions ISO Riluzole promotes the reaction [AR protein binds to SQSTM1 protein] CTD PMID:30280407 NCBI chr10:34,525,517...34,536,670
Ensembl chr10:34,525,519...34,536,673 		JBrowse link
G Tnf tumor necrosis factor multiple interactions ISO [IL6 protein co-treated with IL1A protein co-treated with TNF protein co-treated with lipopolysaccharide, Escherichia coli O111 B4] results in increased susceptibility to Riluzole CTD PMID:19362101 NCBI chr20:3,622,011...3,624,629
Ensembl chr20:3,622,011...3,624,629 		JBrowse link
G Utrn utrophin increases expression ISO Riluzole results in increased expression of UTRN mRNA CTD PMID:22028826 NCBI chr 1:6,720,854...7,224,313
Ensembl chr 1:6,722,594...7,224,313 		JBrowse link
G Vegfa vascular endothelial growth factor A multiple interactions ISO Riluzole inhibits the reaction [VEGFA protein results in increased phosphorylation of PRKCB protein] CTD PMID:16303979 NCBI chr 9:14,955,300...14,970,641
Ensembl chr 9:14,955,300...14,970,641 		JBrowse link
G Xbp1 X-box binding protein 1 increases expression ISO Riluzole results in increased expression of XBP1 protein CTD PMID:30280407 NCBI chr14:80,390,629...80,395,713
Ensembl chr14:80,390,643...80,395,693 		JBrowse link
Sabeluzole term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cyp2d4 cytochrome P450, family 2, subfamily d, polypeptide 4 increases metabolic processing ISO CYP2D6 protein results in increased metabolism of sabeluzole CTD PMID:11259989 NCBI chr 7:113,882,584...113,891,754
Ensembl chr 7:113,881,618...113,891,759 		JBrowse link
saccharin term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Afp alpha-fetoprotein increases expression ISO Saccharin results in increased expression of AFP mRNA CTD PMID:26272751 NCBI chr14:17,573,412...17,591,476
Ensembl chr14:17,573,412...17,591,480 		JBrowse link
G Car13 carbonic anhydrase 13 increases expression ISO Saccharin results in increased expression of CAR13 mRNA CTD PMID:19000923 NCBI chr 2:86,928,401...86,959,525
Ensembl chr 2:86,928,383...86,959,525 		JBrowse link
G Car3 carbonic anhydrase 3 multiple interactions ISO Saccharin binds to and results in decreased activity of CA3 protein CTD PMID:17826101 NCBI chr 2:86,770,418...86,780,011
Ensembl chr 2:86,770,420...86,784,280 		JBrowse link
G Cdk1 cyclin-dependent kinase 1 increases expression ISO Saccharin results in increased expression of CDK1 mRNA CTD PMID:26272751 NCBI chr20:19,266,226...19,281,417
Ensembl chr20:19,266,248...19,281,408 		JBrowse link
G Cer1 cerberus 1, DAN family BMP antagonist increases expression ISO Saccharin results in increased expression of CER1 mRNA CTD PMID:26272751 NCBI chr 5:97,306,427...97,309,783
Ensembl chr 5:97,306,431...97,309,783 		JBrowse link
G Chek1 checkpoint kinase 1 increases expression ISO Saccharin results in increased expression of CHEK1 mRNA CTD PMID:19000923 NCBI chr 8:36,420,565...36,443,477
Ensembl chr 8:36,420,569...36,441,009 		JBrowse link
G Fosl1 FOS like 1, AP-1 transcription factor subunit increases expression ISO Saccharin results in increased expression of FOSL1 mRNA CTD PMID:19000923 NCBI chr 1:202,754,549...202,763,057
Ensembl chr 1:202,754,529...202,764,930 		JBrowse link
G Gnat3 G protein subunit alpha transducin 3 affects response to substance ISO GNAT3 protein affects the susceptibility to Saccharin CTD PMID:16740645 NCBI chr 4:17,162,500...17,212,283
Ensembl chr 4:17,162,490...17,212,283 		JBrowse link
G Hdac7 histone deacetylase 7 decreases expression ISO Saccharin results in decreased expression of HDAC7 mRNA CTD PMID:26272751 NCBI chr 7:128,923,918...128,961,926
Ensembl chr 7:128,923,920...128,962,072 		JBrowse link
G Hells helicase, lymphoid specific increases expression ISO Saccharin results in increased expression of HELLS mRNA CTD PMID:19000923 NCBI chr 1:236,701,704...236,748,239
Ensembl chr 1:236,701,758...236,746,844 		JBrowse link
G Il1rl1 interleukin 1 receptor-like 1 increases expression ISO Saccharin results in increased expression of IL1RL1 mRNA CTD PMID:19000923 NCBI chr 9:42,661,694...42,727,266
Ensembl chr 9:42,697,192...42,727,256 		JBrowse link
G Jun Jun proto-oncogene, AP-1 transcription factor subunit increases expression ISO Saccharin results in increased expression of JUN mRNA CTD PMID:19000923 NCBI chr 5:109,894,175...109,897,268
Ensembl chr 5:109,893,145...109,897,656 		JBrowse link
G Junb JunB proto-oncogene, AP-1 transcription factor subunit increases expression ISO Saccharin results in increased expression of JUNB mRNA CTD PMID:19000923 NCBI chr19:23,176,265...23,178,049
Ensembl chr19:23,176,294...23,178,035 		JBrowse link
G Kdr kinase insert domain receptor increases expression ISO Saccharin results in increased expression of KDR mRNA CTD PMID:26272751 NCBI chr14:32,217,871...32,261,018
Ensembl chr14:32,217,871...32,261,018 		JBrowse link
G Mcm3 minichromosome maintenance complex component 3 increases expression ISO Saccharin results in increased expression of MCM3 mRNA CTD PMID:19000923 NCBI chr 9:23,219,169...23,237,314
Ensembl chr 9:23,219,169...23,237,314 		JBrowse link
G Mesp1 mesoderm posterior bHLH transcription factor 1 decreases expression ISO Saccharin results in decreased expression of MESP1 mRNA CTD PMID:26272751 NCBI chr 1:133,738,357...133,739,875
Ensembl chr 1:133,738,357...133,739,875 		JBrowse link
G Myc MYC proto-oncogene, bHLH transcription factor increases expression ISO Saccharin results in increased expression of MYC mRNA CTD PMID:26272751 NCBI chr 7:93,593,705...93,598,633
Ensembl chr 7:93,593,705...93,598,630 		JBrowse link
G Myo1e myosin IE increases expression ISO Saccharin results in increased expression of MYO1E mRNA CTD PMID:26272751 NCBI chr 8:70,887,934...71,080,180
Ensembl chr 8:70,887,870...71,080,169 		JBrowse link
G Nes nestin increases expression ISO Saccharin results in increased expression of NES mRNA CTD PMID:26272751 NCBI chr 2:173,437,867...173,447,777
Ensembl chr 2:173,438,734...173,447,777 		JBrowse link
G Nos2 nitric oxide synthase 2 increases expression ISO Saccharin results in increased expression of NOS2 mRNA CTD PMID:28472674 NCBI chr10:63,815,308...63,851,208
Ensembl chr10:63,815,308...63,851,210 		JBrowse link
G Nup54 nucleoporin 54 increases expression ISO Saccharin results in increased expression of NUP54 mRNA CTD PMID:19000923 NCBI chr14:15,617,630...15,636,029
Ensembl chr14:15,617,679...15,636,028 		JBrowse link
G Orm1 orosomucoid 1 increases expression ISO Saccharin results in increased expression of ORM1 mRNA CTD PMID:19000923 NCBI chr 5:76,766,637...76,776,149
Ensembl chr 5:76,772,941...76,776,154 		JBrowse link
G Phex phosphate regulating endopeptidase X-linked increases expression ISO Saccharin results in increased expression of PHEX mRNA CTD PMID:19000923 NCBI chr  X:37,607,553...37,856,183
Ensembl chr  X:37,610,760...37,854,469 		JBrowse link
G Pik3r5 phosphoinositide-3-kinase, regulatory subunit 5 increases expression ISO Saccharin results in increased expression of PIK3R5 mRNA CTD PMID:19000923 NCBI chr10:53,132,585...53,200,663
Ensembl chr10:53,132,603...53,199,374 		JBrowse link
G Pnpla6 patatin-like phospholipase domain containing 6 decreases expression ISO Saccharin results in decreased expression of PNPLA6 mRNA CTD PMID:26272751 NCBI chr12:1,574,387...1,603,735
Ensembl chr12:1,560,363...1,603,734 		JBrowse link
G Ppara peroxisome proliferator activated receptor alpha multiple interactions ISO [Saccharin co-treated with Glucose] binds to PPARA protein; Saccharin inhibits the reaction [Glucose inhibits the reaction [Palmitoyl Coenzyme A analog binds to PPARA protein]] CTD PMID:18812576 NCBI chr 7:116,832,405...116,900,878
Ensembl chr 7:116,832,756...116,895,346 		JBrowse link
G Rad21 RAD21 cohesin complex component increases expression ISO Saccharin results in increased expression of RAD21 mRNA CTD PMID:19000923 NCBI chr 7:83,287,867...83,314,810
Ensembl chr 7:83,287,870...83,314,817 		JBrowse link
G Rif1 replication timing regulatory factor 1 increases expression ISO Saccharin results in increased expression of RIF1 mRNA CTD PMID:19000923 NCBI chr 3:36,554,689...36,607,961
Ensembl chr 3:36,554,697...36,603,617 		JBrowse link
G Scarb1 scavenger receptor class B, member 1 increases expression ISO Saccharin results in increased expression of SCARB1 mRNA CTD PMID:19000923 NCBI chr12:31,296,143...31,362,649
Ensembl chr12:31,296,156...31,362,647 		JBrowse link
G Shh sonic hedgehog signaling molecule decreases expression ISO Saccharin results in decreased expression of SHH mRNA CTD PMID:26272751 NCBI chr 4:6,954,017...6,963,170
Ensembl chr 4:6,954,017...6,963,170 		JBrowse link
G Slc2a1 solute carrier family 2 member 1 increases expression ISO Saccharin results in increased expression of SLC2A1 mRNA CTD PMID:19000923 NCBI chr 5:132,717,196...132,745,416
Ensembl chr 5:132,717,196...132,745,416 		JBrowse link
G Stmn1 stathmin 1 increases expression ISO Saccharin results in increased expression of STMN1 mRNA CTD PMID:19000923 NCBI chr 5:146,680,757...146,687,154
Ensembl chr 5:146,681,436...146,687,154 		JBrowse link
G Tas1r3 taste 1 receptor member 3 affects response to substance
multiple interactions		 ISO TAS1R3 protein affects the susceptibility to Saccharin
TRPV1 protein affects the reaction [TAS1R3 protein affects the susceptibility to Saccharin]		 CTD PMID:18804451 NCBI chr 5:166,468,703...166,472,759
Ensembl chr 5:166,469,589...166,472,742 		JBrowse link
G Tas2r136 taste receptor, type 2, member 136 increases activity ISO Saccharin results in increased activity of TAS2R31 protein CTD PMID:21629661 NCBI chr 4:166,098,848...166,099,840
Ensembl chr 4:166,098,848...166,099,840 		JBrowse link
G Tfrc transferrin receptor increases expression ISO Saccharin results in increased expression of TFRC mRNA CTD PMID:19000923 NCBI chr11:68,163,413...68,185,257
Ensembl chr11:68,163,413...68,185,257 		JBrowse link
G Tnf tumor necrosis factor increases expression ISO Saccharin results in increased expression of TNF mRNA CTD PMID:28472674 NCBI chr20:3,622,011...3,624,629
Ensembl chr20:3,622,011...3,624,629 		JBrowse link
G Trpv1 transient receptor potential cation channel, subfamily V, member 1 multiple interactions
increases activity		 ISO TRPV1 protein affects the reaction [TAS1R3 protein affects the susceptibility to Saccharin]
Saccharin results in increased activity of TRPV1 protein		 CTD PMID:17567713 PMID:18804451 NCBI chr10:57,851,428...57,876,513
Ensembl chr10:57,851,428...57,876,513 		JBrowse link
G Vegfa vascular endothelial growth factor A increases expression ISO Saccharin results in increased expression of VEGFA mRNA CTD PMID:19000923 PMID:26272751 NCBI chr 9:14,955,300...14,970,641
Ensembl chr 9:14,955,300...14,970,641 		JBrowse link
G Wnt3 Wnt family member 3 increases expression ISO Saccharin results in increased expression of WNT3 mRNA CTD PMID:26272751 NCBI chr10:88,680,198...88,724,170
Ensembl chr10:88,680,248...88,724,099 		JBrowse link
ziprasidone term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Alb albumin multiple interactions
affects binding		 EXP
ISO		 ziprasidone results in decreased expression of and results in increased reduction of ALB protein
ziprasidone binds to ALB protein
[ziprasidone results in increased reduction of Cysteine] which results in increased activity of ALB protein; stearic acid inhibits the reaction [ziprasidone binds to ALB protein]		 CTD PMID:31400341 NCBI chr14:17,607,397...17,622,814
Ensembl chr14:17,607,381...17,622,836 		JBrowse link
G Cat catalase increases expression EXP ziprasidone results in increased expression of CAT mRNA CTD PMID:32937854 NCBI chr 3:89,842,393...89,874,577
Ensembl chr 3:89,842,399...89,874,478 		JBrowse link
G Hmgcr 3-hydroxy-3-methylglutaryl-CoA reductase increases expression ISO ziprasidone results in increased expression of HMGCR mRNA CTD PMID:17052361 NCBI chr 2:27,997,523...28,018,983
Ensembl chr 2:27,997,525...28,019,703 		JBrowse link
G Hmgcs1 3-hydroxy-3-methylglutaryl-CoA synthase 1 increases expression ISO ziprasidone results in increased expression of HMGCS1 mRNA CTD PMID:17052361 NCBI chr 2:51,649,368...51,667,100
Ensembl chr 2:51,649,497...51,667,100 		JBrowse link
G Hmox1 heme oxygenase 1 increases expression EXP ziprasidone results in increased expression of HMOX1 mRNA CTD PMID:32937854 NCBI chr19:13,466,287...13,474,082
Ensembl chr19:13,467,244...13,474,079 		JBrowse link
G Htr1a 5-hydroxytryptamine receptor 1A multiple interactions EXP [N-(2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl)-N-(2-pyridinyl)cyclohexanecarboxamide binds to and results in decreased activity of HTR1A protein] which results in increased susceptibility to ziprasidone CTD PMID:15996562 NCBI chr 2:36,693,462...36,698,026
Ensembl chr 2:36,694,174...36,695,442 		JBrowse link
G Htr2a 5-hydroxytryptamine receptor 2A multiple interactions ISO ziprasidone inhibits the reaction [Ketanserin binds to HTR2A protein] CTD PMID:16314884 NCBI chr15:49,950,035...50,022,188
Ensembl chr15:49,950,804...50,020,928 		JBrowse link
G Kcnh2 potassium voltage-gated channel subfamily H member 2 decreases activity ISO ziprasidone results in decreased activity of KCNH2 protein CTD PMID:28551711 NCBI chr 4:10,826,834...10,859,009
Ensembl chr 4:10,826,928...10,859,008 		JBrowse link
G Nqo1 NAD(P)H quinone dehydrogenase 1 increases expression EXP ziprasidone results in increased expression of NQO1 mRNA CTD PMID:32937854 NCBI chr19:35,295,633...35,310,528
Ensembl chr19:35,295,573...35,310,557 		JBrowse link
G Sc5d sterol-C5-desaturase increases expression ISO ziprasidone results in increased expression of SC5D mRNA CTD PMID:17052361 NCBI chr 8:42,629,649...42,641,257
Ensembl chr 8:42,632,672...42,641,273 		JBrowse link
G Slc22a5 solute carrier family 22 member 5 multiple interactions ISO ziprasidone inhibits the reaction [SLC22A5 protein results in increased uptake of Carnitine] CTD PMID:30465787 NCBI chr10:38,008,303...38,035,474
Ensembl chr10:38,008,311...38,035,309 		JBrowse link
G Sox17 SRY-box transcription factor 17 decreases localization ISO ziprasidone results in decreased localization of SOX17 protein CTD PMID:24154490 NCBI chr 5:15,016,660...15,022,228
Ensembl chr 5:15,016,731...15,022,228 		JBrowse link
Term paths to the root
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Term Annotations click to browse term
  CHEBI ontology 19874
    chemical entity 19872
      atom 19872
        nonmetal atom 19794
          nitrogen atom 18974
            nitrogen molecular entity 18974
              organonitrogen compound 18827
                organonitrogen heterocyclic compound 18148
                  benzothiazoles 151
                    (2E)-5-(1,3-Benzothiazol-2-yl)-2-[(E)-3-[5-(1,3-benzothiazol-2-yl)-3-ethyl-1,3-benzothiazol-3-ium-2-yl]prop-2-enylidene]-3-ethyl-1,3-benzothiazole 0
                    (2S,4R)-1-acetyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-(benzothiazol-2-ylcarbonyl)butyl]-4-hydroxypyrrolidine-2-carboxamide 0
                    (2Z)-3-Ethyl-2-[[(3Z)-3-[(E)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-5-methylcyclohexen-1-yl]methylidene]-1,3-benzothiazole 0
                    (4,7-dichloro-1,3-benzothiazol-2-yl)hydrazine 0
                    (4-oxo-3-\{[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl\}-3,4-dihydrophthalazin-1-yl)acetic acid 16
                    (5-fluoro-2-\{[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]carbamoyl\}phenoxy)acetic acid 0
                    (5S)-5-\{4-[(2S)-2-(1H-benzimidazol-2-yl)-2-(1,3-benzothiazol-2-ylamino)ethyl]phenyl\}isothiazolidin-3-one 1,1-dioxide 0
                    (7S)-2-[(carboxycarbonyl)amino]-7-\{[(1,1-dioxido-1,2-benzothiazol-3-yl)oxy]methyl\}-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid 0
                    (S)-4,5-dihydro-2-(6-hydroxy-1,3-benzothiazol-2-yl)-1,3-thiazole-4-carboxylic acid 0
                    1,2-benzisothiazole + 51
                    1,3-Benzothiazol-2-ylmethanol 0
                    1,3-benzothiazol-2-yl(thiomorpholin-4-yl)methanone 0
                    1,3-benzothiazole-2-sulfonamide 0
                    1,3-benzothiazole-2-thiol + 52
                    1,3-benzothiazole-6-carboxylic acid (2-benzamido-2-oxoethyl) ester 0
                    1,3-benzothiazole-6-carboxylic acid [2-(2-furanyl)-2-oxoethyl] ester 0
                    1,3-benzothiazole-6-carboxylic acid [2-[(3,5-dichloro-4-methyl-2-pyridinyl)amino]-2-oxoethyl] ester 0
                    1,3-benzothiazole-6-carboxylic acid [2-[1-(1-methoxypropan-2-yl)-2,5-dimethyl-3-pyrrolyl]-2-oxoethyl] ester 0
                    1-(1,1-dioxo-1,2-benzothiazol-3-yl)-N-(2-methylphenyl)-4-piperidinecarboxamide 0
                    1-(1,3-benzothiazol-2-yl)-3-propylurea 0
                    1-(2-furanylmethyl)-N-[2-(methylthio)-1,3-benzothiazol-6-yl]-5-oxo-3-pyrrolidinecarboxamide 0
                    1-(4-amino-1,2,5-oxadiazol-3-yl)-5-[(1,3-benzothiazol-2-ylthio)methyl]-4-triazolecarboxylic acid methyl ester 0
                    1-[(1,3-benzothiazol-2-ylthio)methyl]-2-azepanone 0
                    1-[(3S)-3-(1,3-Benzothiazol-2-yl)-1-pyrrolidinyl]-2-phenoxyethanone 0
                    1-[[2-(1,3-benzothiazol-2-ylthio)-1-oxoethyl]amino]-3-phenylthiourea 0
                    1-cyclohexyl-3-(6-ethoxy-1,3-benzothiazol-2-yl)urea 0
                    1-methyl-3-oxo-1,3-dihydro-2,1-benzothiazole-5-sulfonamide 0
                    1-thiophen-2-ylsulfonyl-4-piperidinecarboxylic acid 1,3-benzothiazol-2-ylmethyl ester 0
                    2,2-dimethyl-N-(6-methyl-1,3-benzothiazol-2-yl)propanamide 0
                    2,5-Dimethylbenzothiazole 0
                    2-(1,3-benzothiazol-2-yl)-2-[2-[2-(3-pyridinyl)ethylamino]-4-pyrimidinyl]acetonitrile 0
                    2-(1,3-benzothiazol-2-yl)-3-(1,4-dioxo-1,2,3,4-tetrahydrophthalazin-6-yl)-5-[(E)-2-phenylethenyl]-2H-tetrazol-3-ium 0
                    2-(1,3-benzothiazol-2-yl)-3-methyl-2-butenenitrile 0
                    2-(1,3-benzothiazol-2-yl)-4-chloro-3-oxo-4-phenylbutanenitrile 0
                    2-(1,3-benzothiazol-2-yl)-4-chloro-5-(3-chloroanilino)-3-pyridazinone 0
                    2-(1,3-benzothiazol-2-yl)-4-fluorophenol + 0
                    2-(1,3-benzothiazol-2-yl)-5-methyl-3-pyrazolamine 0
                    2-(1,3-benzothiazol-2-yl)phenol 0
                    2-(1,3-benzothiazol-2-ylmethoxy)phenol 0
                    2-(1,3-benzothiazol-2-ylmethylthio)-1-butyl-5-benzimidazolesulfonamide 0
                    2-(1H-benzimidazol-2-yl)-1,3-benzothiazole 0
                    2-(2,4,5-trimethoxyphenyl)-1,3-benzothiazole 0
                    2-(2,4-dichlorophenyl)-1,2-benzothiazol-3-one 0
                    2-(2,4-dimethylphenyl)-6-fluoro-1,2-benzothiazol-3-one 0
                    2-(2,5-dimethylphenyl)-6-fluoro-1,2-benzothiazol-3-one 0
                    2-(2-chloro-3-pyridinyl)-1,3-benzothiazole 0
                    2-(2-chlorophenyl)-5-fluoro-1,2-benzothiazol-3-one 0
                    2-(2-fluorophenyl)-1,2-benzothiazol-3-one 0
                    2-(2-oxo-1,3-benzothiazol-3-yl)-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)acetamide 0
                    2-(3,5-dimethyl-1H-pyrrol-2-yl)-1,3-benzothiazole 0
                    2-(3-chlorophenyl)-1,2-benzothiazol-3-one 0
                    2-(3-fluorophenyl)-1-oxo-1,2-benzothiazol-3-one 0
                    2-(3-oxo-1,2-benzothiazol-2-yl)-N-phenylacetamide 0
                    2-(4,5-dihydrothiazol-2-ylthio)-N-(6-methoxy-1,3-benzothiazol-2-yl)acetamide 0
                    2-(4-Morpholinyl)benzothiazole 0
                    2-(4-chlorophenoxy)-N-[3-(dimethylamino)propyl]-N-(4-methoxy-1,3-benzothiazol-2-yl)acetamide 0
                    2-(4-chlorophenoxy)-N-[3-(dimethylamino)propyl]-N-(4-methyl-1,3-benzothiazol-2-yl)acetamide 0
                    2-(4-chlorophenyl)-1,2-benzothiazol-3-one 0
                    2-(4-fluorophenyl)-1,2-benzothiazol-3-one 0
                    2-(4-fluorophenyl)-6-methoxy-1,3-benzothiazole 0
                    2-(4-methoxyphenyl)-1,2-benzothiazol-3-one 0
                    2-(6-imidazo[2,1-b]thiazolyl)acetic acid 1,3-benzothiazol-2-ylmethyl ester 0
                    2-(6-imidazo[2,1-b]thiazolyl)acetic acid [2-(1,3-benzothiazol-2-ylamino)-2-oxoethyl] ester 0
                    2-(Methylthio)-1,3-benzothiazol-6-amine 0
                    2-(\{[4-(6-methyl-1,3-benzothiazol-2-yl)phenyl]imino\}methyl)phenol 0
                    2-(beta-D-glucosyl)benzothiazole 0
                    2-Butylbenzothiazole 0
                    2-Heptylbenzothiazole 0
                    2-Hexylbenzothiazole 0
                    2-L-arginyl-1,3-benzothiazole-6-carboxylic acid 0
                    2-[(1-cyclohexyl-5-tetrazolyl)thio]-N-(6-ethoxy-1,3-benzothiazol-2-yl)acetamide 0
                    2-[(2-chlorophenyl)methylthio]-6-nitro-1,3-benzothiazole 0
                    2-[(3-bromo-2-imidazo[1,2-a]pyrimidinyl)methylthio]-1,3-benzothiazole 0
                    2-[(3S)-1-(2-Pyridinylmethyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                    2-[(3S)-1-(2-Thienylmethyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                    2-[(3S)-1-(3,4-Difluorobenzyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                    2-[(3S)-1-(3-Methoxybenzyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                    2-[(3S)-1-Benzyl-3-pyrrolidinyl]-1,3-benzothiazole 0
                    2-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-4-thiazolecarboxylic acid ethyl ester 0
                    2-[2-(1,3-benzothiazol-2-ylsulfonyl)ethylthio]-4,6-dimethyl-3-pyridinecarbonitrile 0
                    2-[5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl(oxo)methyl]-1,1-dioxo-1,2-benzothiazol-3-one 0
                    2-[[3-[4-(dimethylamino)phenyl]-4,5-dihydroisoxazol-5-yl]methyl]-1,1-dioxo-1,2-benzothiazol-3-one 0
                    2-[[4-methyl-5-[(2-oxo-1,3-benzothiazol-3-yl)methyl]-1,2,4-triazol-3-yl]thio]-N-(phenylmethyl)acetamide 0
                    2-[[5-[(1,3-benzothiazol-2-ylthio)methyl]-4-methyl-1,2,4-triazol-3-yl]thio]-N-[2-(4-morpholinyl)ethyl]acetamide 0
                    2-[[6-[(3-bromo-6-oxo-1-cyclohexa-2,4-dienylidene)methylamino]-1,3-benzothiazol-2-yl]thio]-N-phenylacetamide 0
                    2-[[cyclohexyl(oxo)methyl]amino]-1,3-benzothiazole-6-carboxylic acid methyl ester 0
                    2-aminobenzothiazole + 0
                    2-benzothiazolsulfonic acid 0
                    2-chloro-N-(3-methyl-1,3-benzothiazol-2-ylidene)acetamide 0
                    2-methylthio-1,3-benzothiazole 0
                    2-phenyl-5-(trifluoromethyl)-1,2-benzothiazol-3-one 0
                    2-pyridin-4-yl-1,3-benzothiazole 0
                    3,4,5-trimethoxy-N-(3-methyl-1,3-benzothiazol-2-ylidene)benzamide 0
                    3-(1,3-Benzothiazol-2-ylthio)pentane-2,4-dione 0
                    3-(1,3-benzothiazol-2-yl)-2-methoxypropanoic acid 0
                    3-(1,3-benzothiazol-2-yl)propanoic acid (3,5-dimethyl-4-isoxazolyl)methyl ester 0
                    3-(1,3-benzothiazol-2-ylsulfanyl)propane-1-sulfonic acid 0
                    3-(1,3-benzothiazol-2-ylthio)-N-[(4-methoxyphenyl)methylideneamino]propanamide 0
                    3-(2-phenoxyethyl)-1,3-benzothiazol-2-one 0
                    3-(3,5-dimethyl-1-pyrazolyl)-1,2-benzothiazole 1,1-dioxide 0
                    3-(benzenesulfonyl)-N-[2-(diethylamino)ethyl]-N-(4,6-dimethyl-1,3-benzothiazol-2-yl)propanamide 0
                    3-(benzenesulfonyl)-N-[4-(6-methyl-1,3-benzothiazol-2-yl)phenyl]propanamide 0
                    3-(benzothiazol-2-yl)-7-(diethylamino)-2-oxo-2H-1-benzopyran-4-carbonitrile 0
                    3-[(1,3-benzothiazol-2-ylthio)methyl]-4-cyclohexyl-1H-1,2,4-triazole-5-thione 0
                    3-[2-(3-ethyl-4-oxo-2-sulfanylidene-5-thiazolidinylidene)-1,3-benzothiazol-3-yl]-1-propanesulfonic acid 0
                    3-[2-(3-methylphenoxy)ethyl]-1,3-benzothiazol-2-one 0
                    3-[2-(4-methylphenoxy)ethyl]-1,3-benzothiazol-2-one 0
                    3-[2-[(E,3E)-3-(3-Ethyl-5-methoxy-1,3-benzothiazol-2-ylidene)-2-methoxyprop-1-enyl]-1,3-benzothiazol-3-ium-3-yl]propane-1-sulfonate 0
                    3-[3-(2-methoxyphenoxy)propyl]-1,3-benzothiazol-2-one 0
                    3-[3-(4-tert-butylphenoxy)propyl]-1,3-benzothiazol-2-one 0
                    3-[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]-2-(1,3-benzothiazol-2-yl)-2-propenenitrile 0
                    3-[4-(2-methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzyl]-1,3-benzothiazol-2(3H)-one 0
                    3-\{[(3S)-3-(1,3-Benzothiazol-2-yl)-1-pyrrolidinyl]methyl\}benzonitrile 0
                    3-chloro-N-[3-(2-methoxyethyl)-6-sulfamoyl-1,3-benzothiazol-2-ylidene]-1-benzothiophene-2-carboxamide 0
                    3-ethyl-2-[(2Z)-2-(3-ethyl-6-sulfo-1,3-benzothiazol-2(3H)-ylidene)hydrazino]-6-sulfo-3H-1,3-benzothiazol-1-ium 0
                    3-methoxy-N-(3-methyl-6-methylsulfonyl-1,3-benzothiazol-2-ylidene)benzamide 0
                    3-methoxy-N-(6-methylsulfonyl-1,3-benzothiazol-2-yl)benzamide 0
                    3-oxo-2-phenyl-1,2-benzothiazole-5-carbonitrile 0
                    3-oxo-2-phenyl-1,2-benzothiazole-6-carbonitrile 0
                    4-(1,3-benzothiazol-2-yl)-5-(4-chloro-3-nitrophenyl)-4-pentenoic acid 0
                    4-(1,3-benzothiazol-2-ylthio)butanoic acid [2-[(3-cyano-2-thiophenyl)amino]-2-oxoethyl] ester 0
                    4-(4,6-difluoro-1,3-benzothiazol-2-yl)morpholine 0
                    4-[(5-chloro-1,3-benzothiazol-2-yl)thio]-2-(1-iminoethyl)-3-oxobutanenitrile 0
                    4-[[1-(6-ethoxy-1,3-benzothiazol-2-yl)-3-piperidinyl]-oxomethyl]-1-piperazinecarboxylic acid ethyl ester 0
                    4-[[2-(4-methyl-1-piperidinyl)-1,3-benzothiazol-6-yl]-oxomethyl]-1-piperazinecarboxylic acid ethyl ester 0
                    4-[[5-(1,3-benzothiazol-2-yl)-2-thiophenyl]-oxomethyl]-1-piperazinecarboxaldehyde 0
                    4-fluoro-N-(4-fluoro-1,3-benzothiazol-2-yl)-1,3-benzothiazol-2-amine 0
                    5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl)-1,3-benzothiazol-6-yl hydrogen sulfate 0
                    5-(5-methoxy-3-methyl-1,3-benzothiazol-2-ylidene)-2-(phenylmethyl)imino-3-prop-2-enyl-4-thiazolidinone 0
                    5-[(1,3-benzothiazol-2-ylthio)methyl]-2-furancarboxylic acid methyl ester 0
                    5-[(4-chloro-1-pyrazolyl)methyl]-N-(6-methyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    5-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-3-methyl-2-thiophenecarboxylic acid ethyl ester 0
                    5-amino-4-(1,3-benzothiazol-2-yl)-1-cyclohexyl-2H-pyrrol-3-one 0
                    5-amino-4-(1,3-benzothiazol-6-ylhydrazinylidene)-2-phenyl-3-pyrazolone 0
                    5-bromo-2-thiophenecarboxylic acid 1,3-benzothiazol-2-ylmethyl ester 0
                    5-bromo-N-(4,7-dimethoxy-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    5-bromo-N-(4-methoxy-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    5-bromo-N-(6-butyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    5-bromo-N-(6-sulfamoyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    5-bromo-N-[3-(dimethylamino)propyl]-N-(4,5-dimethyl-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    5-fluoro-2-phenyl-1,2-benzothiazol-3-one 0
                    5-heptyl-6-hydroxy-1,3-benzothiazole-4,7-dione 0
                    5-nitro-2-phenyl-1,2-benzothiazol-3-one 0
                    6-(2-amino-2-carboxyethyl)-4-hydroxybenzothiazole 0
                    6-Fluoro-1,3-benzothiazol-2-amine 0
                    6-[2-(diethylamino)ethoxy]-N,N-dimethyl-1,3-benzothiazol-2-amine 0
                    6-[4-(6-bromo-1,2-benzothiazol-3-yl)phenoxy]-N-methyl-N-prop-2-en-1-ylhexan-1-amine 0
                    6-\{[3-(4-bromophenyl)-1,2-benzothiazol-6-yl]oxy\}-N-methyl-N-prop-2-en-1-ylhexan-1-amine 0
                    6-bromo-2-(1-pyrrolidinyl)-1,3-benzothiazole 0
                    6-ethoxy-2-[(4-fluorophenyl)methylthio]-1,3-benzothiazole 0
                    6-fluoro-2-(2-methylphenyl)-1,2-benzothiazol-3-one 0
                    6-fluoro-2-phenyl-1,2-benzothiazol-3-one 0
                    6-fluoro-N-phenyl-1,3-benzothiazol-2-amine 0
                    6-hydroxy-1,3-benzothiazole-2-sulfonamide 0
                    6-hydroxy-5-undecyl-1,3-benzothiazole-4,7-dione 0
                    6-methoxy-3-methyl-1,3-benzothiazol-2-imine 0
                    6-nitro-2-phenyl-1,2-benzothiazol-3-one 0
                    6-propan-2-yl-1,3-benzothiazol-2-amine 0
                    8-methoxy-3-(phenylmethyl)pyrimido[2,1-b][1,3]benzothiazole-2,4-dione 0
                    Benzthiazuron 0
                    C3-thiacarbocyanine 0
                    C3-thiacarbocyanine cation + 1
                    C545T 0
                    Diamthazole dihydrochloride 0
                    E3040 + 3
                    E3040 glucuronide 0
                    INDY + 0
                    ML355 0
                    Methabenzthiazuron 0
                    Methyl 2-(6-hydroxybenzothiazol-4-yl) acetate 0
                    N'-(4,5-dimethyl-1,3-benzothiazol-2-yl)propanehydrazide 0
                    N'-(4,6-difluoro-1,3-benzothiazol-2-yl)benzohydrazide 0
                    N'-(4,6-difluoro-1,3-benzothiazol-2-yl)propanehydrazide 0
                    N'-(4-fluoro-1,3-benzothiazol-2-yl)-2-phenoxyacetohydrazide 0
                    N'-(4-methoxy-1,3-benzothiazol-2-yl)-N,N-dimethyliminoformamide 0
                    N'-(6-methoxy-1,3-benzothiazol-2-yl)-N,N-dimethylmethanimidamide 0
                    N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzamide 0
                    N-(1,3-benzothiazol-2-yl)-2-[(1-methyl-2-imidazolyl)thio]acetamide 0
                    N-(1,3-benzothiazol-2-yl)-2-cyclohexylacetamide 0
                    N-(1,3-benzothiazol-2-yl)-2-methoxy-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]benzamide 0
                    N-(1,3-benzothiazol-2-yl)-2-oxolanecarboxamide 0
                    N-(1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    N-(1,3-benzothiazol-2-yl)-N-methylbenzamide 0
                    N-(2-furanylmethyl)-2-(2-oxo-1,3-benzothiazol-3-yl)acetamide 0
                    N-(2-methyl-1,3-benzothiazol-6-yl)-2-furancarboxamide 0
                    N-(2-methyl-1,3-benzothiazol-6-yl)benzamide 0
                    N-(2-oxolanylmethyl)-2-(1-piperidinyl)-1,3-benzothiazole-6-carboxamide 0
                    N-(2-phenylethyl)-1,3-benzothiazol-2-amine 0
                    N-(3-methyl-1,3-benzothiazol-2-ylidene)-2-pyrazinecarboxamide 0
                    N-(3-oxo-2-phenyl-1,2-benzothiazol-5-yl)acetamide 0
                    N-(3-oxo-2-phenyl-1,2-benzothiazol-6-yl)acetamide 0
                    N-(3-phenyl-1,3-benzothiazol-2-ylidene)-2-propenamide 0
                    N-(4,5,6-trifluoro-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    N-(4,6-dimethyl-2-pyrimidinyl)-1,3-benzothiazol-2-amine 0
                    N-(4,7-dimethoxy-3-methyl-1,3-benzothiazol-2-ylidene)butanamide 0
                    N-(4-bromophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                    N-(4-chlorophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                    N-(4-fluoro-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    N-(4-fluoro-3-methyl-1,3-benzothiazol-2-ylidene)-2-nitrobenzamide 0
                    N-(4-fluorophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                    N-(4-methoxyphenyl)-1,3-benzothiazol-2-amine 0
                    N-(4-methoxyphenyl)-3-methyl-1,3-benzothiazol-2-imine 0
                    N-(4-methyl-1,3-benzothiazol-2-yl)-2-(1-pyrrolyl)acetamide 0
                    N-(4-methyl-2-thiazolyl)-3-(2-oxo-1,3-benzothiazol-3-yl)propanamide 0
                    N-(4-methylphenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                    N-(5-methoxy-1,3-benzothiazol-2-yl)-3-methylbutanamide 0
                    N-(5-phenyl-1,3,4-oxadiazol-2-yl)-1,3-benzothiazole-2-carboxamide 0
                    N-(6-acetamido-3-prop-2-enyl-1,3-benzothiazol-2-ylidene)-2-thiophenecarboxamide 0
                    N-(6-acetamido-3-prop-2-enyl-1,3-benzothiazol-2-ylidene)cyclohexanecarboxamide 0
                    N-(6-butyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    N-(6-butyl-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                    N-(6-chloro-1,3-benzothiazol-2-yl)-1,5-dimethyl-3-pyrazolecarboxamide 0
                    N-(6-chloro-1,3-benzothiazol-2-yl)-2-diphenylphosphorylacetamide 0
                    N-(6-ethoxy-1,3-benzothiazol-2-yl)-1,3-dimethyl-2-oxo-5-benzimidazolesulfonamide 0
                    N-(6-ethoxy-1,3-benzothiazol-2-yl)-2-methoxyacetamide 0
                    N-(6-ethoxy-1,3-benzothiazol-2-yl)butanamide 0
                    N-(6-fluoro-1,3-benzothiazol-2-yl)-2-oxolanecarboxamide 0
                    N-(6-methoxy-1,3-benzothiazol-2-yl)-1-thiophen-2-ylsulfonyl-4-piperidinecarboxamide 0
                    N-(6-methyl-1,3-benzothiazol-2-yl)-2-(5,6,7,8-tetrahydro-4H-cyclohepta[c]pyrazol-2-yl)acetamide 0
                    N-(6-methyl-1,3-benzothiazol-2-yl)-6-oxo-1-phenyl-4,5-dihydropyridazine-3-carboxamide 0
                    N-(6-methylsulfonyl-1,3-benzothiazol-2-yl)-4-oxo-4-thiophen-2-ylbutanamide 0
                    N-(7-methyl-2-thiazolo[4,5-g][1,3]benzothiazolyl)propanamide 0
                    N-(benzylsulfonyl)-3-cyclohexyl-D-alanyl-N-(2-amino-1,3-benzothiazol-6-yl)-L-prolinamide 0
                    N-Methylbenzothiazole-2-thione 0
                    N-[(1S)-1-(1,3-benzothiazol-2-ylcarbonyl)-4-carbamimidamidobutyl]cyclopentanecarboxamide 0
                    N-[(2R,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3R)-5-[(2S)-1-hydroxypropan-2-yl]-2-[[(4-methoxyphenyl)methyl-methylamino]methyl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3S)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3S)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3S)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl-(phenylmethyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2R,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3R)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3R)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3R)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3S)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(2S,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                    N-[(3-nitro-4-\{[2-(phenylsulfanyl)ethyl]amino\}phenyl)sulfonyl]-4-[2-(2-phenylethyl)-1,3-benzothiazol-5-yl]benzamide 0
                    N-[1-(1,3-benzodioxol-5-yl)ethylideneamino]-1,3-benzothiazol-2-amine 0
                    N-[2-(1,3-benzothiazol-2-ylthio)-1-oxoethyl]-1-methyl-2-pyrrolecarboxamide 0
                    N-[2-(1-azepanyl)-1,3-benzothiazol-6-yl]carbamic acid ethyl ester 0
                    N-[2-(1-cyclohexenyl)ethyl]-3-(2-oxo-1,3-benzothiazol-3-yl)propanamide 0
                    N-[2-(5-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)ethenyl]-N-methylaniline 0
                    N-[2-(dimethylamino)ethyl]-N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)cyclohexanecarboxamide 0
                    N-[2-(methylthio)-1,3-benzothiazol-6-yl]-2-furancarboxamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-2-yl]-2,2,2-trifluoroacetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-5,6,7,8-tetrahydro-4H-thieno[2,3-c]azepin-2-yl]acetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-5,6-dihydro-4H-thieno[2,3-c]pyrrol-2-yl]acetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-5-propan-2-yl-4,6-dihydrothieno[2,3-c]pyrrol-2-yl]acetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-6-propan-2-yl-4,5,7,8-tetrahydrothieno[2,3-d]azepin-2-yl]acetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-6-propan-2-yl-5,7-dihydro-4H-thieno[2,3-c]pyridin-2-yl]-2,2,2-trifluoroacetamide 0
                    N-[3-(1,3-benzothiazol-2-yl)-7-propan-2-yl-4,5,6,8-tetrahydrothieno[2,3-c]azepin-2-yl]acetamide 0
                    N-[3-(2-methoxyethyl)-6-methylsulfonyl-1,3-benzothiazol-2-ylidene]-2-nitrobenzamide 0
                    N-[3-(2-methylcyclohexyl)-2,4-dihydro-1H-1,3,5-triazin-6-yl]-1,3-benzothiazol-2-amine 0
                    N-[3-(3,5-dimethyl-1-piperidinyl)propyl]-2-(1-piperidinyl)-1,3-benzothiazole-6-carboxamide 0
                    N-[3-(3H-1,3-benzothiazol-2-ylidene)-4-oxo-1-cyclohexa-1,5-dienyl]-3-methyl-2-thiophenecarboxamide 0
                    N-[3-(4-bromophenyl)prop-2-enylideneamino]-1,3-benzothiazol-2-amine 0
                    N-[3-(dimethylamino)propyl]-N-(4-fluoro-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                    N-[3-(dimethylamino)propyl]-N-(6-methyl-1,3-benzothiazol-2-yl)-1,3-benzothiazole-6-carboxamide 0
                    N-[3-(dimethylamino)propyl]-N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)-5-nitro-2-furancarboxamide 0
                    N-[4,6-bis(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(methylthio)-1,3-benzothiazol-6-amine 0
                    N-[6-(diethylsulfamoyl)-1,3-benzothiazol-2-yl]-2-thiophenecarboxamide 0
                    N-[6-(dimethylsulfamoyl)-1,3-benzothiazol-2-yl]-2-thiophenecarboxamide 0
                    N-[[(6-methoxy-1,3-benzothiazol-2-yl)amino]-sulfanylidenemethyl]-2-furancarboxamide 0
                    N-[[(6-methyl-1,3-benzothiazol-2-yl)amino]-sulfanylidenemethyl]-2-thiophenecarboxamide 0
                    N-\{4-[2-ethyl-1-(1,2,4-triazol-1-yl)butyl]phenyl\}-1,3-benzothiazol-2-amine + 0
                    N-cyclohexyl-2-(methylthio)-1,3-benzothiazole-6-sulfonamide 0
                    N-cyclohexyl-2-benzothiazol-amine 0
                    NVP-231 0
                    Photinus luciferin + 0
                    PicoGreen 0
                    Pronqodine A 0
                    Riluzole 28
                    S 1319 0
                    SZL-P1-41 0
                    Sabeluzole 1
                    TAK-632 0
                    Tiaramide hydrochloride 0
                    Tozadenant 0
                    [4-(butan-2-ylamino)-6-chloro-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                    [4-chloro-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                    [4-methoxy-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                    [\{4-[(2R,4E)-2-(1,3-benzothiazol-2-yl)-2-(1H-benzotriazol-1-yl)-5-phenylpent-4-en-1-yl]phenyl\}(difluoro)methyl]phosphonic acid 0
                    \{3-[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]-1H-indol-1-yl\}acetic acid 0
                    alcian yellow cation + 0
                    aspirin-based probe AP 0
                    benazolin + 0
                    benazolin-ethyl 0
                    benthiavalicarb + 0
                    benthiavalicarb-isopropyl 0
                    benzothiazole + 5
                    benzothiazole fungicide + 0
                    dehydroluciferin 0
                    dibenzothiazol-2-yl disulfide 2
                    dithiazanine + 1
                    dithiazanine iodide 0
                    ent-Photinus luciferin + 0
                    ethoxzolamide 3
                    firefly sulfoluciferin 0
                    flutemetamol ((18)F) 0
                    haletazole 0
                    lubeluzole 1
                    mefenacet 3
                    methyl (2E)-1,3-benzothiazol-2(3H)-ylidene(cyano)acetate 0
                    pramipexole 10
                    primuline (acid form) 0
                    proINDY 0
                    ryuvidine 0
                    tiaramide 0
                    ticlatone 0
                    tioxidazole 0
                    tyrphostin AG 825 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19874
    subatomic particle 19872
      composite particle 19872
        hadron 19872
          baryon 19872
            nucleon 19872
              atomic nucleus 19872
                atom 19872
                  main group element atom 19811
                    p-block element atom 19811
                      carbon group element atom 19751
                        carbon atom 19748
                          organic molecular entity 19748
                            organic molecule 19700
                              organic cyclic compound 19490
                                organic heterocyclic compound 18868
                                  organic heteropolycyclic compound 18294
                                    organic heterobicyclic compound 17237
                                      benzothiazoles 151
                                        (2E)-5-(1,3-Benzothiazol-2-yl)-2-[(E)-3-[5-(1,3-benzothiazol-2-yl)-3-ethyl-1,3-benzothiazol-3-ium-2-yl]prop-2-enylidene]-3-ethyl-1,3-benzothiazole 0
                                        (2S,4R)-1-acetyl-N-[(1S)-4-[(aminoiminomethyl)amino]-1-(benzothiazol-2-ylcarbonyl)butyl]-4-hydroxypyrrolidine-2-carboxamide 0
                                        (2Z)-3-Ethyl-2-[[(3Z)-3-[(E)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-5-methylcyclohexen-1-yl]methylidene]-1,3-benzothiazole 0
                                        (4,7-dichloro-1,3-benzothiazol-2-yl)hydrazine 0
                                        (4-oxo-3-\{[5-(trifluoromethyl)-1,3-benzothiazol-2-yl]methyl\}-3,4-dihydrophthalazin-1-yl)acetic acid 16
                                        (5-fluoro-2-\{[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]carbamoyl\}phenoxy)acetic acid 0
                                        (5S)-5-\{4-[(2S)-2-(1H-benzimidazol-2-yl)-2-(1,3-benzothiazol-2-ylamino)ethyl]phenyl\}isothiazolidin-3-one 1,1-dioxide 0
                                        (7S)-2-[(carboxycarbonyl)amino]-7-\{[(1,1-dioxido-1,2-benzothiazol-3-yl)oxy]methyl\}-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid 0
                                        (S)-4,5-dihydro-2-(6-hydroxy-1,3-benzothiazol-2-yl)-1,3-thiazole-4-carboxylic acid 0
                                        1,2-benzisothiazole + 51
                                        1,3-Benzothiazol-2-ylmethanol 0
                                        1,3-benzothiazol-2-yl(thiomorpholin-4-yl)methanone 0
                                        1,3-benzothiazole-2-sulfonamide 0
                                        1,3-benzothiazole-2-thiol + 52
                                        1,3-benzothiazole-6-carboxylic acid (2-benzamido-2-oxoethyl) ester 0
                                        1,3-benzothiazole-6-carboxylic acid [2-(2-furanyl)-2-oxoethyl] ester 0
                                        1,3-benzothiazole-6-carboxylic acid [2-[(3,5-dichloro-4-methyl-2-pyridinyl)amino]-2-oxoethyl] ester 0
                                        1,3-benzothiazole-6-carboxylic acid [2-[1-(1-methoxypropan-2-yl)-2,5-dimethyl-3-pyrrolyl]-2-oxoethyl] ester 0
                                        1-(1,1-dioxo-1,2-benzothiazol-3-yl)-N-(2-methylphenyl)-4-piperidinecarboxamide 0
                                        1-(1,3-benzothiazol-2-yl)-3-propylurea 0
                                        1-(2-furanylmethyl)-N-[2-(methylthio)-1,3-benzothiazol-6-yl]-5-oxo-3-pyrrolidinecarboxamide 0
                                        1-(4-amino-1,2,5-oxadiazol-3-yl)-5-[(1,3-benzothiazol-2-ylthio)methyl]-4-triazolecarboxylic acid methyl ester 0
                                        1-[(1,3-benzothiazol-2-ylthio)methyl]-2-azepanone 0
                                        1-[(3S)-3-(1,3-Benzothiazol-2-yl)-1-pyrrolidinyl]-2-phenoxyethanone 0
                                        1-[[2-(1,3-benzothiazol-2-ylthio)-1-oxoethyl]amino]-3-phenylthiourea 0
                                        1-cyclohexyl-3-(6-ethoxy-1,3-benzothiazol-2-yl)urea 0
                                        1-methyl-3-oxo-1,3-dihydro-2,1-benzothiazole-5-sulfonamide 0
                                        1-thiophen-2-ylsulfonyl-4-piperidinecarboxylic acid 1,3-benzothiazol-2-ylmethyl ester 0
                                        2,2-dimethyl-N-(6-methyl-1,3-benzothiazol-2-yl)propanamide 0
                                        2,5-Dimethylbenzothiazole 0
                                        2-(1,3-benzothiazol-2-yl)-2-[2-[2-(3-pyridinyl)ethylamino]-4-pyrimidinyl]acetonitrile 0
                                        2-(1,3-benzothiazol-2-yl)-3-(1,4-dioxo-1,2,3,4-tetrahydrophthalazin-6-yl)-5-[(E)-2-phenylethenyl]-2H-tetrazol-3-ium 0
                                        2-(1,3-benzothiazol-2-yl)-3-methyl-2-butenenitrile 0
                                        2-(1,3-benzothiazol-2-yl)-4-chloro-3-oxo-4-phenylbutanenitrile 0
                                        2-(1,3-benzothiazol-2-yl)-4-chloro-5-(3-chloroanilino)-3-pyridazinone 0
                                        2-(1,3-benzothiazol-2-yl)-4-fluorophenol + 0
                                        2-(1,3-benzothiazol-2-yl)-5-methyl-3-pyrazolamine 0
                                        2-(1,3-benzothiazol-2-yl)phenol 0
                                        2-(1,3-benzothiazol-2-ylmethoxy)phenol 0
                                        2-(1,3-benzothiazol-2-ylmethylthio)-1-butyl-5-benzimidazolesulfonamide 0
                                        2-(1H-benzimidazol-2-yl)-1,3-benzothiazole 0
                                        2-(2,4,5-trimethoxyphenyl)-1,3-benzothiazole 0
                                        2-(2,4-dichlorophenyl)-1,2-benzothiazol-3-one 0
                                        2-(2,4-dimethylphenyl)-6-fluoro-1,2-benzothiazol-3-one 0
                                        2-(2,5-dimethylphenyl)-6-fluoro-1,2-benzothiazol-3-one 0
                                        2-(2-chloro-3-pyridinyl)-1,3-benzothiazole 0
                                        2-(2-chlorophenyl)-5-fluoro-1,2-benzothiazol-3-one 0
                                        2-(2-fluorophenyl)-1,2-benzothiazol-3-one 0
                                        2-(2-oxo-1,3-benzothiazol-3-yl)-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)acetamide 0
                                        2-(3,5-dimethyl-1H-pyrrol-2-yl)-1,3-benzothiazole 0
                                        2-(3-chlorophenyl)-1,2-benzothiazol-3-one 0
                                        2-(3-fluorophenyl)-1-oxo-1,2-benzothiazol-3-one 0
                                        2-(3-oxo-1,2-benzothiazol-2-yl)-N-phenylacetamide 0
                                        2-(4,5-dihydrothiazol-2-ylthio)-N-(6-methoxy-1,3-benzothiazol-2-yl)acetamide 0
                                        2-(4-Morpholinyl)benzothiazole 0
                                        2-(4-chlorophenoxy)-N-[3-(dimethylamino)propyl]-N-(4-methoxy-1,3-benzothiazol-2-yl)acetamide 0
                                        2-(4-chlorophenoxy)-N-[3-(dimethylamino)propyl]-N-(4-methyl-1,3-benzothiazol-2-yl)acetamide 0
                                        2-(4-chlorophenyl)-1,2-benzothiazol-3-one 0
                                        2-(4-fluorophenyl)-1,2-benzothiazol-3-one 0
                                        2-(4-fluorophenyl)-6-methoxy-1,3-benzothiazole 0
                                        2-(4-methoxyphenyl)-1,2-benzothiazol-3-one 0
                                        2-(6-imidazo[2,1-b]thiazolyl)acetic acid 1,3-benzothiazol-2-ylmethyl ester 0
                                        2-(6-imidazo[2,1-b]thiazolyl)acetic acid [2-(1,3-benzothiazol-2-ylamino)-2-oxoethyl] ester 0
                                        2-(Methylthio)-1,3-benzothiazol-6-amine 0
                                        2-(\{[4-(6-methyl-1,3-benzothiazol-2-yl)phenyl]imino\}methyl)phenol 0
                                        2-(beta-D-glucosyl)benzothiazole 0
                                        2-Butylbenzothiazole 0
                                        2-Heptylbenzothiazole 0
                                        2-Hexylbenzothiazole 0
                                        2-L-arginyl-1,3-benzothiazole-6-carboxylic acid 0
                                        2-[(1-cyclohexyl-5-tetrazolyl)thio]-N-(6-ethoxy-1,3-benzothiazol-2-yl)acetamide 0
                                        2-[(2-chlorophenyl)methylthio]-6-nitro-1,3-benzothiazole 0
                                        2-[(3-bromo-2-imidazo[1,2-a]pyrimidinyl)methylthio]-1,3-benzothiazole 0
                                        2-[(3S)-1-(2-Pyridinylmethyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                                        2-[(3S)-1-(2-Thienylmethyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                                        2-[(3S)-1-(3,4-Difluorobenzyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                                        2-[(3S)-1-(3-Methoxybenzyl)-3-pyrrolidinyl]-1,3-benzothiazole 0
                                        2-[(3S)-1-Benzyl-3-pyrrolidinyl]-1,3-benzothiazole 0
                                        2-[(6-fluoro-1,3-benzothiazol-2-yl)amino]-4-thiazolecarboxylic acid ethyl ester 0
                                        2-[2-(1,3-benzothiazol-2-ylsulfonyl)ethylthio]-4,6-dimethyl-3-pyridinecarbonitrile 0
                                        2-[5,6-dihydro-4H-cyclopenta[b]thiophen-2-yl(oxo)methyl]-1,1-dioxo-1,2-benzothiazol-3-one 0
                                        2-[[3-[4-(dimethylamino)phenyl]-4,5-dihydroisoxazol-5-yl]methyl]-1,1-dioxo-1,2-benzothiazol-3-one 0
                                        2-[[4-methyl-5-[(2-oxo-1,3-benzothiazol-3-yl)methyl]-1,2,4-triazol-3-yl]thio]-N-(phenylmethyl)acetamide 0
                                        2-[[5-[(1,3-benzothiazol-2-ylthio)methyl]-4-methyl-1,2,4-triazol-3-yl]thio]-N-[2-(4-morpholinyl)ethyl]acetamide 0
                                        2-[[6-[(3-bromo-6-oxo-1-cyclohexa-2,4-dienylidene)methylamino]-1,3-benzothiazol-2-yl]thio]-N-phenylacetamide 0
                                        2-[[cyclohexyl(oxo)methyl]amino]-1,3-benzothiazole-6-carboxylic acid methyl ester 0
                                        2-aminobenzothiazole + 0
                                        2-benzothiazolsulfonic acid 0
                                        2-chloro-N-(3-methyl-1,3-benzothiazol-2-ylidene)acetamide 0
                                        2-methylthio-1,3-benzothiazole 0
                                        2-phenyl-5-(trifluoromethyl)-1,2-benzothiazol-3-one 0
                                        2-pyridin-4-yl-1,3-benzothiazole 0
                                        3,4,5-trimethoxy-N-(3-methyl-1,3-benzothiazol-2-ylidene)benzamide 0
                                        3-(1,3-Benzothiazol-2-ylthio)pentane-2,4-dione 0
                                        3-(1,3-benzothiazol-2-yl)-2-methoxypropanoic acid 0
                                        3-(1,3-benzothiazol-2-yl)propanoic acid (3,5-dimethyl-4-isoxazolyl)methyl ester 0
                                        3-(1,3-benzothiazol-2-ylsulfanyl)propane-1-sulfonic acid 0
                                        3-(1,3-benzothiazol-2-ylthio)-N-[(4-methoxyphenyl)methylideneamino]propanamide 0
                                        3-(2-phenoxyethyl)-1,3-benzothiazol-2-one 0
                                        3-(3,5-dimethyl-1-pyrazolyl)-1,2-benzothiazole 1,1-dioxide 0
                                        3-(benzenesulfonyl)-N-[2-(diethylamino)ethyl]-N-(4,6-dimethyl-1,3-benzothiazol-2-yl)propanamide 0
                                        3-(benzenesulfonyl)-N-[4-(6-methyl-1,3-benzothiazol-2-yl)phenyl]propanamide 0
                                        3-(benzothiazol-2-yl)-7-(diethylamino)-2-oxo-2H-1-benzopyran-4-carbonitrile 0
                                        3-[(1,3-benzothiazol-2-ylthio)methyl]-4-cyclohexyl-1H-1,2,4-triazole-5-thione 0
                                        3-[2-(3-ethyl-4-oxo-2-sulfanylidene-5-thiazolidinylidene)-1,3-benzothiazol-3-yl]-1-propanesulfonic acid 0
                                        3-[2-(3-methylphenoxy)ethyl]-1,3-benzothiazol-2-one 0
                                        3-[2-(4-methylphenoxy)ethyl]-1,3-benzothiazol-2-one 0
                                        3-[2-[(E,3E)-3-(3-Ethyl-5-methoxy-1,3-benzothiazol-2-ylidene)-2-methoxyprop-1-enyl]-1,3-benzothiazol-3-ium-3-yl]propane-1-sulfonate 0
                                        3-[3-(2-methoxyphenoxy)propyl]-1,3-benzothiazol-2-one 0
                                        3-[3-(4-tert-butylphenoxy)propyl]-1,3-benzothiazol-2-one 0
                                        3-[4-(1,3-benzodioxol-5-ylmethyl)-1-piperazinyl]-2-(1,3-benzothiazol-2-yl)-2-propenenitrile 0
                                        3-[4-(2-methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzyl]-1,3-benzothiazol-2(3H)-one 0
                                        3-\{[(3S)-3-(1,3-Benzothiazol-2-yl)-1-pyrrolidinyl]methyl\}benzonitrile 0
                                        3-chloro-N-[3-(2-methoxyethyl)-6-sulfamoyl-1,3-benzothiazol-2-ylidene]-1-benzothiophene-2-carboxamide 0
                                        3-ethyl-2-[(2Z)-2-(3-ethyl-6-sulfo-1,3-benzothiazol-2(3H)-ylidene)hydrazino]-6-sulfo-3H-1,3-benzothiazol-1-ium 0
                                        3-methoxy-N-(3-methyl-6-methylsulfonyl-1,3-benzothiazol-2-ylidene)benzamide 0
                                        3-methoxy-N-(6-methylsulfonyl-1,3-benzothiazol-2-yl)benzamide 0
                                        3-oxo-2-phenyl-1,2-benzothiazole-5-carbonitrile 0
                                        3-oxo-2-phenyl-1,2-benzothiazole-6-carbonitrile 0
                                        4-(1,3-benzothiazol-2-yl)-5-(4-chloro-3-nitrophenyl)-4-pentenoic acid 0
                                        4-(1,3-benzothiazol-2-ylthio)butanoic acid [2-[(3-cyano-2-thiophenyl)amino]-2-oxoethyl] ester 0
                                        4-(4,6-difluoro-1,3-benzothiazol-2-yl)morpholine 0
                                        4-[(5-chloro-1,3-benzothiazol-2-yl)thio]-2-(1-iminoethyl)-3-oxobutanenitrile 0
                                        4-[[1-(6-ethoxy-1,3-benzothiazol-2-yl)-3-piperidinyl]-oxomethyl]-1-piperazinecarboxylic acid ethyl ester 0
                                        4-[[2-(4-methyl-1-piperidinyl)-1,3-benzothiazol-6-yl]-oxomethyl]-1-piperazinecarboxylic acid ethyl ester 0
                                        4-[[5-(1,3-benzothiazol-2-yl)-2-thiophenyl]-oxomethyl]-1-piperazinecarboxaldehyde 0
                                        4-fluoro-N-(4-fluoro-1,3-benzothiazol-2-yl)-1,3-benzothiazol-2-amine 0
                                        5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl)-1,3-benzothiazol-6-yl hydrogen sulfate 0
                                        5-(5-methoxy-3-methyl-1,3-benzothiazol-2-ylidene)-2-(phenylmethyl)imino-3-prop-2-enyl-4-thiazolidinone 0
                                        5-[(1,3-benzothiazol-2-ylthio)methyl]-2-furancarboxylic acid methyl ester 0
                                        5-[(4-chloro-1-pyrazolyl)methyl]-N-(6-methyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        5-[(6-methoxy-1,3-benzothiazol-2-yl)amino]-3-methyl-2-thiophenecarboxylic acid ethyl ester 0
                                        5-amino-4-(1,3-benzothiazol-2-yl)-1-cyclohexyl-2H-pyrrol-3-one 0
                                        5-amino-4-(1,3-benzothiazol-6-ylhydrazinylidene)-2-phenyl-3-pyrazolone 0
                                        5-bromo-2-thiophenecarboxylic acid 1,3-benzothiazol-2-ylmethyl ester 0
                                        5-bromo-N-(4,7-dimethoxy-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        5-bromo-N-(4-methoxy-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        5-bromo-N-(6-butyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        5-bromo-N-(6-sulfamoyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        5-bromo-N-[3-(dimethylamino)propyl]-N-(4,5-dimethyl-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        5-fluoro-2-phenyl-1,2-benzothiazol-3-one 0
                                        5-heptyl-6-hydroxy-1,3-benzothiazole-4,7-dione 0
                                        5-nitro-2-phenyl-1,2-benzothiazol-3-one 0
                                        6-(2-amino-2-carboxyethyl)-4-hydroxybenzothiazole 0
                                        6-Fluoro-1,3-benzothiazol-2-amine 0
                                        6-[2-(diethylamino)ethoxy]-N,N-dimethyl-1,3-benzothiazol-2-amine 0
                                        6-[4-(6-bromo-1,2-benzothiazol-3-yl)phenoxy]-N-methyl-N-prop-2-en-1-ylhexan-1-amine 0
                                        6-\{[3-(4-bromophenyl)-1,2-benzothiazol-6-yl]oxy\}-N-methyl-N-prop-2-en-1-ylhexan-1-amine 0
                                        6-bromo-2-(1-pyrrolidinyl)-1,3-benzothiazole 0
                                        6-ethoxy-2-[(4-fluorophenyl)methylthio]-1,3-benzothiazole 0
                                        6-fluoro-2-(2-methylphenyl)-1,2-benzothiazol-3-one 0
                                        6-fluoro-2-phenyl-1,2-benzothiazol-3-one 0
                                        6-fluoro-N-phenyl-1,3-benzothiazol-2-amine 0
                                        6-hydroxy-1,3-benzothiazole-2-sulfonamide 0
                                        6-hydroxy-5-undecyl-1,3-benzothiazole-4,7-dione 0
                                        6-methoxy-3-methyl-1,3-benzothiazol-2-imine 0
                                        6-nitro-2-phenyl-1,2-benzothiazol-3-one 0
                                        6-propan-2-yl-1,3-benzothiazol-2-amine 0
                                        8-methoxy-3-(phenylmethyl)pyrimido[2,1-b][1,3]benzothiazole-2,4-dione 0
                                        Benzthiazuron 0
                                        C3-thiacarbocyanine 0
                                        C3-thiacarbocyanine cation + 1
                                        C545T 0
                                        Diamthazole dihydrochloride 0
                                        E3040 + 3
                                        E3040 glucuronide 0
                                        INDY + 0
                                        ML355 0
                                        Methabenzthiazuron 0
                                        Methyl 2-(6-hydroxybenzothiazol-4-yl) acetate 0
                                        N'-(4,5-dimethyl-1,3-benzothiazol-2-yl)propanehydrazide 0
                                        N'-(4,6-difluoro-1,3-benzothiazol-2-yl)benzohydrazide 0
                                        N'-(4,6-difluoro-1,3-benzothiazol-2-yl)propanehydrazide 0
                                        N'-(4-fluoro-1,3-benzothiazol-2-yl)-2-phenoxyacetohydrazide 0
                                        N'-(4-methoxy-1,3-benzothiazol-2-yl)-N,N-dimethyliminoformamide 0
                                        N'-(6-methoxy-1,3-benzothiazol-2-yl)-N,N-dimethylmethanimidamide 0
                                        N,N-dimethyl-3-(3-oxo-1,2-benzothiazol-2-yl)benzamide 0
                                        N-(1,3-benzothiazol-2-yl)-2-[(1-methyl-2-imidazolyl)thio]acetamide 0
                                        N-(1,3-benzothiazol-2-yl)-2-cyclohexylacetamide 0
                                        N-(1,3-benzothiazol-2-yl)-2-methoxy-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]benzamide 0
                                        N-(1,3-benzothiazol-2-yl)-2-oxolanecarboxamide 0
                                        N-(1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        N-(1,3-benzothiazol-2-yl)-N-methylbenzamide 0
                                        N-(2-furanylmethyl)-2-(2-oxo-1,3-benzothiazol-3-yl)acetamide 0
                                        N-(2-methyl-1,3-benzothiazol-6-yl)-2-furancarboxamide 0
                                        N-(2-methyl-1,3-benzothiazol-6-yl)benzamide 0
                                        N-(2-oxolanylmethyl)-2-(1-piperidinyl)-1,3-benzothiazole-6-carboxamide 0
                                        N-(2-phenylethyl)-1,3-benzothiazol-2-amine 0
                                        N-(3-methyl-1,3-benzothiazol-2-ylidene)-2-pyrazinecarboxamide 0
                                        N-(3-oxo-2-phenyl-1,2-benzothiazol-5-yl)acetamide 0
                                        N-(3-oxo-2-phenyl-1,2-benzothiazol-6-yl)acetamide 0
                                        N-(3-phenyl-1,3-benzothiazol-2-ylidene)-2-propenamide 0
                                        N-(4,5,6-trifluoro-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        N-(4,6-dimethyl-2-pyrimidinyl)-1,3-benzothiazol-2-amine 0
                                        N-(4,7-dimethoxy-3-methyl-1,3-benzothiazol-2-ylidene)butanamide 0
                                        N-(4-bromophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                                        N-(4-chlorophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                                        N-(4-fluoro-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        N-(4-fluoro-3-methyl-1,3-benzothiazol-2-ylidene)-2-nitrobenzamide 0
                                        N-(4-fluorophenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                                        N-(4-methoxyphenyl)-1,3-benzothiazol-2-amine 0
                                        N-(4-methoxyphenyl)-3-methyl-1,3-benzothiazol-2-imine 0
                                        N-(4-methyl-1,3-benzothiazol-2-yl)-2-(1-pyrrolyl)acetamide 0
                                        N-(4-methyl-2-thiazolyl)-3-(2-oxo-1,3-benzothiazol-3-yl)propanamide 0
                                        N-(4-methylphenyl)-2-(3-oxo-1,2-benzothiazol-2-yl)acetamide 0
                                        N-(5-methoxy-1,3-benzothiazol-2-yl)-3-methylbutanamide 0
                                        N-(5-phenyl-1,3,4-oxadiazol-2-yl)-1,3-benzothiazole-2-carboxamide 0
                                        N-(6-acetamido-3-prop-2-enyl-1,3-benzothiazol-2-ylidene)-2-thiophenecarboxamide 0
                                        N-(6-acetamido-3-prop-2-enyl-1,3-benzothiazol-2-ylidene)cyclohexanecarboxamide 0
                                        N-(6-butyl-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        N-(6-butyl-1,3-benzothiazol-2-yl)-2-thiophenecarboxamide 0
                                        N-(6-chloro-1,3-benzothiazol-2-yl)-1,5-dimethyl-3-pyrazolecarboxamide 0
                                        N-(6-chloro-1,3-benzothiazol-2-yl)-2-diphenylphosphorylacetamide 0
                                        N-(6-ethoxy-1,3-benzothiazol-2-yl)-1,3-dimethyl-2-oxo-5-benzimidazolesulfonamide 0
                                        N-(6-ethoxy-1,3-benzothiazol-2-yl)-2-methoxyacetamide 0
                                        N-(6-ethoxy-1,3-benzothiazol-2-yl)butanamide 0
                                        N-(6-fluoro-1,3-benzothiazol-2-yl)-2-oxolanecarboxamide 0
                                        N-(6-methoxy-1,3-benzothiazol-2-yl)-1-thiophen-2-ylsulfonyl-4-piperidinecarboxamide 0
                                        N-(6-methyl-1,3-benzothiazol-2-yl)-2-(5,6,7,8-tetrahydro-4H-cyclohepta[c]pyrazol-2-yl)acetamide 0
                                        N-(6-methyl-1,3-benzothiazol-2-yl)-6-oxo-1-phenyl-4,5-dihydropyridazine-3-carboxamide 0
                                        N-(6-methylsulfonyl-1,3-benzothiazol-2-yl)-4-oxo-4-thiophen-2-ylbutanamide 0
                                        N-(7-methyl-2-thiazolo[4,5-g][1,3]benzothiazolyl)propanamide 0
                                        N-(benzylsulfonyl)-3-cyclohexyl-D-alanyl-N-(2-amino-1,3-benzothiazol-6-yl)-L-prolinamide 0
                                        N-Methylbenzothiazole-2-thione 0
                                        N-[(1S)-1-(1,3-benzothiazol-2-ylcarbonyl)-4-carbamimidamidobutyl]cyclopentanecarboxamide 0
                                        N-[(2R,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3R)-5-[(2S)-1-hydroxypropan-2-yl]-2-[[(4-methoxyphenyl)methyl-methylamino]methyl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3S)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3S)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3S)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-[[methyl-(phenylmethyl)amino]methyl]-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2R,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3R)-2-[[(3,4-dichlorophenyl)methyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3R)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3R)-2-[[(3,5-dimethyl-4-isoxazolyl)sulfonyl-methylamino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3R)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3R)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3S)-2-[[cyclopropylmethyl(methyl)amino]methyl]-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3S)-5-[(2R)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(2S,3S)-5-[(2S)-1-hydroxypropan-2-yl]-3-methyl-2-(methylaminomethyl)-6-oxo-3,4-dihydro-2H-1,5-benzoxazocin-10-yl]-1,3-benzothiazole-2-carboxamide 0
                                        N-[(3-nitro-4-\{[2-(phenylsulfanyl)ethyl]amino\}phenyl)sulfonyl]-4-[2-(2-phenylethyl)-1,3-benzothiazol-5-yl]benzamide 0
                                        N-[1-(1,3-benzodioxol-5-yl)ethylideneamino]-1,3-benzothiazol-2-amine 0
                                        N-[2-(1,3-benzothiazol-2-ylthio)-1-oxoethyl]-1-methyl-2-pyrrolecarboxamide 0
                                        N-[2-(1-azepanyl)-1,3-benzothiazol-6-yl]carbamic acid ethyl ester 0
                                        N-[2-(1-cyclohexenyl)ethyl]-3-(2-oxo-1,3-benzothiazol-3-yl)propanamide 0
                                        N-[2-(5-chloro-3-ethyl-1,3-benzothiazol-3-ium-2-yl)ethenyl]-N-methylaniline 0
                                        N-[2-(dimethylamino)ethyl]-N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)cyclohexanecarboxamide 0
                                        N-[2-(methylthio)-1,3-benzothiazol-6-yl]-2-furancarboxamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-2-yl]-2,2,2-trifluoroacetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-5,6,7,8-tetrahydro-4H-thieno[2,3-c]azepin-2-yl]acetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-5,6-dihydro-4H-thieno[2,3-c]pyrrol-2-yl]acetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-5-propan-2-yl-4,6-dihydrothieno[2,3-c]pyrrol-2-yl]acetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-6-propan-2-yl-4,5,7,8-tetrahydrothieno[2,3-d]azepin-2-yl]acetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-6-propan-2-yl-5,7-dihydro-4H-thieno[2,3-c]pyridin-2-yl]-2,2,2-trifluoroacetamide 0
                                        N-[3-(1,3-benzothiazol-2-yl)-7-propan-2-yl-4,5,6,8-tetrahydrothieno[2,3-c]azepin-2-yl]acetamide 0
                                        N-[3-(2-methoxyethyl)-6-methylsulfonyl-1,3-benzothiazol-2-ylidene]-2-nitrobenzamide 0
                                        N-[3-(2-methylcyclohexyl)-2,4-dihydro-1H-1,3,5-triazin-6-yl]-1,3-benzothiazol-2-amine 0
                                        N-[3-(3,5-dimethyl-1-piperidinyl)propyl]-2-(1-piperidinyl)-1,3-benzothiazole-6-carboxamide 0
                                        N-[3-(3H-1,3-benzothiazol-2-ylidene)-4-oxo-1-cyclohexa-1,5-dienyl]-3-methyl-2-thiophenecarboxamide 0
                                        N-[3-(4-bromophenyl)prop-2-enylideneamino]-1,3-benzothiazol-2-amine 0
                                        N-[3-(dimethylamino)propyl]-N-(4-fluoro-1,3-benzothiazol-2-yl)-2-furancarboxamide 0
                                        N-[3-(dimethylamino)propyl]-N-(6-methyl-1,3-benzothiazol-2-yl)-1,3-benzothiazole-6-carboxamide 0
                                        N-[3-(dimethylamino)propyl]-N-([1,3]dioxolo[4,5-f][1,3]benzothiazol-6-yl)-5-nitro-2-furancarboxamide 0
                                        N-[4,6-bis(4-morpholinyl)-1,3,5-triazin-2-yl]-2-(methylthio)-1,3-benzothiazol-6-amine 0
                                        N-[6-(diethylsulfamoyl)-1,3-benzothiazol-2-yl]-2-thiophenecarboxamide 0
                                        N-[6-(dimethylsulfamoyl)-1,3-benzothiazol-2-yl]-2-thiophenecarboxamide 0
                                        N-[[(6-methoxy-1,3-benzothiazol-2-yl)amino]-sulfanylidenemethyl]-2-furancarboxamide 0
                                        N-[[(6-methyl-1,3-benzothiazol-2-yl)amino]-sulfanylidenemethyl]-2-thiophenecarboxamide 0
                                        N-\{4-[2-ethyl-1-(1,2,4-triazol-1-yl)butyl]phenyl\}-1,3-benzothiazol-2-amine + 0
                                        N-cyclohexyl-2-(methylthio)-1,3-benzothiazole-6-sulfonamide 0
                                        N-cyclohexyl-2-benzothiazol-amine 0
                                        NVP-231 0
                                        Photinus luciferin + 0
                                        PicoGreen 0
                                        Pronqodine A 0
                                        Riluzole 28
                                        S 1319 0
                                        SZL-P1-41 0
                                        Sabeluzole 1
                                        TAK-632 0
                                        Tiaramide hydrochloride 0
                                        Tozadenant 0
                                        [4-(butan-2-ylamino)-6-chloro-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                                        [4-chloro-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                                        [4-methoxy-6-(propan-2-ylamino)-1,3,5-triazin-2-yl]-[(1,1,3-trioxo-1,2-benzothiazol-2-yl)methyl]cyanamide 0
                                        [\{4-[(2R,4E)-2-(1,3-benzothiazol-2-yl)-2-(1H-benzotriazol-1-yl)-5-phenylpent-4-en-1-yl]phenyl\}(difluoro)methyl]phosphonic acid 0
                                        \{3-[(4,5,7-trifluoro-1,3-benzothiazol-2-yl)methyl]-1H-indol-1-yl\}acetic acid 0
                                        alcian yellow cation + 0
                                        aspirin-based probe AP 0
                                        benazolin + 0
                                        benazolin-ethyl 0
                                        benthiavalicarb + 0
                                        benthiavalicarb-isopropyl 0
                                        benzothiazole + 5
                                        benzothiazole fungicide + 0
                                        dehydroluciferin 0
                                        dibenzothiazol-2-yl disulfide 2
                                        dithiazanine + 1
                                        dithiazanine iodide 0
                                        ent-Photinus luciferin + 0
                                        ethoxzolamide 3
                                        firefly sulfoluciferin 0
                                        flutemetamol ((18)F) 0
                                        haletazole 0
                                        lubeluzole 1
                                        mefenacet 3
                                        methyl (2E)-1,3-benzothiazol-2(3H)-ylidene(cyano)acetate 0
                                        pramipexole 10
                                        primuline (acid form) 0
                                        proINDY 0
                                        ryuvidine 0
                                        tiaramide 0
                                        ticlatone 0
                                        tioxidazole 0
                                        tyrphostin AG 825 0
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