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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:indol-3-ylacetaldehyde
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Accession:CHEBI:18086 term browser browse the term
Definition:An indoleacetaldehyde that is acetaldehyde in which one of the methyl hydrogens are replaced by a indol-3-yl group. It is an intermediate metabolite in the metabolism of tryptophan.
Synonyms:related_synonym: 1H-Indol-3-ylacetaldehyde;   1H-Indole-3-acetaldehyde;   2-(Indol-3-yl)acetaldehyde;   Formula=C10H9NO;   InChI=1S/C10H9NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,6-7,11H,5H2;   InChIKey=WHOOUMGHGSPMGR-UHFFFAOYSA-N;   Indoleacetaldehyde;   SMILES=O=CCc1c[nH]c2ccccc12;   indole-3-acetaldehyde
 alt_id: CHEBI:11477;   CHEBI:14445;   CHEBI:24798;   CHEBI:5902
 xref: CAS:2591-98-2;   HMDB:HMDB0001190;   KEGG:C00637;   KNApSAcK:C00000109
 xref_mesh: MESH:C001655
 xref: MetaCyc:INDOLE_ACETALDEHYDE;   PMID:20217460;   PMID:22274708;   PMID:4015706;   PMID:4031860;   PMID:6862384;   Reaxys:121586


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indol-3-ylacetaldehyde term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cyp1a1 cytochrome P450, family 1, subfamily a, polypeptide 1 decreases activity ISO indole-3-acetaldehyde metabolite results in decreased activity of CYP1A1 protein CTD PMID:26686552 NCBI chr 8:66,991,940...66,998,014
Ensembl chr 8:66,991,970...66,998,012 		JBrowse link
G Maoa monoamine oxidase A multiple interactions
increases chemical synthesis 		ISO [[MAOA protein results in decreased amination of tryptamine] which results in increased chemical synthesis of indole-3-acetaldehyde] which results in increased chemical synthesis of 6-formylindolo(3,2-b)carbazole; [MAOA protein results in decreased amination of tryptamine] which results in increased chemical synthesis of indole-3-acetaldehyde
MAOA protein results in increased chemical synthesis of indole-3-acetaldehyde 		CTD PMID:26686552 NCBI chr  X:8,615,239...8,681,372
Ensembl chr  X:8,615,239...8,682,631 		JBrowse link
G Maob monoamine oxidase B multiple interactions
increases chemical synthesis 		ISO [[MAOB protein results in decreased amination of tryptamine] which results in increased chemical synthesis of indole-3-acetaldehyde] which results in increased chemical synthesis of 6-formylindolo(3,2-b)carbazole; [MAOB protein results in decreased amination of tryptamine] which results in increased chemical synthesis of indole-3-acetaldehyde
MAOB protein results in increased chemical synthesis of indole-3-acetaldehyde 		CTD PMID:26686552 NCBI chr  X:8,490,405...8,594,065
Ensembl chr  X:8,490,344...8,594,375 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 20862
    role 20820
      chemical role 20396
        oxidising agent 12057
          acetaldehyde 561
            indoleacetaldehyde 3
              indol-3-ylacetaldehyde 3
Path 2
Term Annotations click to browse term
  CHEBI ontology 20862
    subatomic particle 20860
      composite particle 20860
        hadron 20860
          baryon 20860
            nucleon 20860
              atomic nucleus 20860
                atom 20860
                  main group element atom 20781
                    p-block element atom 20781
                      carbon group element atom 20715
                        carbon atom 20710
                          organic molecular entity 20710
                            heteroorganic entity 20219
                              organochalcogen compound 19904
                                organooxygen compound 19806
                                  carbon oxoacid 19155
                                    carboxylic acid 19152
                                      carboacyl group 18085
                                        univalent carboacyl group 18085
                                          formyl group 9407
                                            aldehyde 9407
                                              acetaldehyde 561
                                                indoleacetaldehyde 3
                                                  indol-3-ylacetaldehyde 3
paths to the root