Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

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:acetophenone
go back to main search page
Accession:CHEBI:27632 term browser browse the term
Definition:A methyl ketone that is acetone in which one of the methyl groups has been replaced by a phenyl group.
Synonyms:related_synonym: 1-Phenylethan-1-one;   1-Phenylethanone;   Acetylbenzene;   Formula=C8H8O;   InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3;   InChIKey=KWOLFJPFCHCOCG-UHFFFAOYSA-N;   Methyl phenyl ketone;   SMILES=CC(=O)c1ccccc1;   benzoyl methide
 alt_id: CHEBI:22186;   CHEBI:2403;   CHEBI:40490
 xref: CAS:98-86-2;   DrugBank:DB04619;   HMDB:HMDB0033910;   KEGG:C07113;   KNApSAcK:C00002685
 xref_mesh: MESH:C038699
 xref: PMID:10397882;   PMID:24634568;   UM-BBD_compID:c0117;   Wikipedia:Acetophenone


show annotations for term's descendants           Sort by:
acetophenone term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aldh2 aldehyde dehydrogenase 2 family member multiple interactions ISO acetophenone inhibits the reaction [4-dimethylaminocinnamaldehyde binds to ALDH2 protein] CTD PMID:10609638 NCBI chr12:34,949,549...34,982,527
Ensembl chr12:34,901,219...34,982,521 		JBrowse link
G Alpp alkaline phosphatase, placental increases chemical synthesis ISO ALPP protein results in increased chemical synthesis of acetophenone CTD PMID:1495895 NCBI chr 9:87,765,846...87,768,606
Ensembl chr 9:87,765,860...87,768,606 		JBrowse link
G Esr2 estrogen receptor 2 multiple interactions ISO acetophenone binds to and results in decreased activity of ESR2 protein CTD PMID:27633901 NCBI chr 6:94,858,438...94,909,630
Ensembl chr 6:94,809,547...94,908,919 		JBrowse link
G Or8a1b olfactory receptor family 8 subfamily A member 1B multiple interactions
increases activity		 ISO acetophenone binds to and results in increased activity of OR8A1 protein
acetophenone results in increased activity of OR8A1 protein		 CTD PMID:11943806 PMID:19052201 NCBI chr 8:37,434,903...37,435,832
Ensembl chr 8:37,434,551...37,439,746 		JBrowse link
G Pparg peroxisome proliferator-activated receptor gamma multiple interactions ISO acetophenone binds to and results in decreased activity of PPARG protein CTD PMID:27633901 NCBI chr 4:148,423,102...148,548,471
Ensembl chr 4:148,423,194...148,548,468 		JBrowse link
G Trpa1 transient receptor potential cation channel, subfamily A, member 1 increases activity ISO acetophenone results in increased activity of TRPA1 protein CTD PMID:27545873 NCBI chr 5:4,379,862...4,434,133
Ensembl chr 5:4,379,999...4,433,570 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19898
    role 19868
      biological role 19866
        xenobiotic 18753
          acetophenone 6
            2-methoxyacetophenone 0
            2-phenoxyacetophenone 0
            3,4,5-trimethoxyacetophenone 0
            4-acetoxy acetophenone 0
            4-hydroxy-3-methylacetophenone 0
            N-acetyl-S-phenacyl-L-cysteine 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19898
    subatomic particle 19896
      composite particle 19896
        hadron 19896
          baryon 19896
            nucleon 19896
              atomic nucleus 19896
                atom 19896
                  main group element atom 19835
                    p-block element atom 19835
                      carbon group element atom 19774
                        carbon atom 19771
                          organic molecular entity 19771
                            heteroorganic entity 19528
                              organochalcogen compound 19290
                                organooxygen compound 19206
                                  carbonyl compound 18929
                                    ketone 17272
                                      methyl ketone 845
                                        acetophenones 162
                                          acetophenone 6
                                            2-methoxyacetophenone 0
                                            2-phenoxyacetophenone 0
                                            3,4,5-trimethoxyacetophenone 0
                                            4-acetoxy acetophenone 0
                                            4-hydroxy-3-methylacetophenone 0
                                            N-acetyl-S-phenacyl-L-cysteine 0
paths to the root