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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:indole-3-butyric acid
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Accession:CHEBI:33070 term browser browse the term
Definition:A indol-3-yl carboxylic acid that is butanoic acid carrying a 1H-indol-3-yl substituent at position 1.
Synonyms:exact_synonym: 4-(1H-indol-3-yl)butanoic acid
 related_synonym: 1H-indole-3-butanoic acid;   3-INDOLEBUTYRIC ACID;   3-indolyl-gamma-butyric acid;   4-(indol-3-yl)butyric acid;   4-indol-3-ylbutyric acid;   Formula=C12H13NO2;   IBA;   InChI=1S/C12H13NO2/c14-12(15)7-3-4-9-8-13-11-6-2-1-5-10(9)11/h1-2,5-6,8,13H,3-4,7H2,(H,14,15);   InChIKey=JTEDVYBZBROSJT-UHFFFAOYSA-N;   Indolebutyric acid;   SMILES=OC(=O)CCCc1c[nH]c2ccccc12;   Seradix;   indole-3-butanoic acid
 alt_id: CHEBI:24806;   CHEBI:39986;   CHEBI:5914
 xref: BPDB:1465;   Beilstein:171120;   CAS:133-32-4;   DrugBank:DB02740;   Gmelin:143637;   HMDB:HMDB0002096;   KEGG:C11284;   KNApSAcK:C00000116
 xref_mesh: MESH:C014612
 xref: PDBeChem:3IB;   PMID:23201417;   PMID:23795714;   Reaxys:171120;   Wikipedia:Indole-3-butyric_acid
 cyclic_relationship: is_conjugate_acid_of CHEBI:143274


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indole-3-butyric acid term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ache acetylcholinesterase decreases activity EXP indolebutyric acid results in decreased activity of ACHE protein CTD PMID:19442822 NCBI chr12:22,472,358...22,477,052
Ensembl chr12:22,472,358...22,478,753
JBrowse link
G Ada adenosine deaminase decreases activity EXP indolebutyric acid results in decreased activity of ADA protein CTD PMID:19442822 NCBI chr 3:160,115,840...160,139,947
Ensembl chr 3:160,115,842...160,139,947
JBrowse link
G Bche butyrylcholinesterase decreases activity EXP indolebutyric acid results in decreased activity of BCHE protein CTD PMID:19442822 NCBI chr 2:171,104,476...171,196,186
Ensembl chr 2:171,100,140...171,196,395
JBrowse link
G Mpo myeloperoxidase increases activity EXP indolebutyric acid results in increased activity of MPO protein CTD PMID:19442822 NCBI chr10:75,087,892...75,098,260
Ensembl chr10:75,087,892...75,098,260
JBrowse link
G Nfkbia NFKB inhibitor alpha increases expression ISO indolebutyric acid analog results in increased expression of NFKBIA protein CTD PMID:23499788 NCBI chr 6:76,267,227...76,270,457
Ensembl chr 6:76,267,228...76,270,457
JBrowse link
G Parp1 poly (ADP-ribose) polymerase 1 increases cleavage ISO indolebutyric acid analog results in increased cleavage of PARP1 protein CTD PMID:23499788 NCBI chr13:98,857,255...98,889,444
Ensembl chr13:98,857,177...98,889,716
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19816
    role 19764
      biological role 19764
        molecular messenger 18279
          hormone 18031
            plant hormone 4919
              indole-3-butyric acid 6
                4-(indol-3-yl)butanoyl-beta-D-glucose 0
                N(2)-[4-(indol-3-yl)butanoyl]-L-glutamine 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19816
    subatomic particle 19814
      composite particle 19814
        hadron 19814
          baryon 19814
            nucleon 19814
              atomic nucleus 19814
                atom 19814
                  main group element atom 19702
                    p-block element atom 19702
                      carbon group element atom 19608
                        carbon atom 19597
                          organic molecular entity 19597
                            organic group 18537
                              organic divalent group 18530
                                organodiyl group 18530
                                  carbonyl group 18436
                                    carbonyl compound 18436
                                      carboxylic acid 18114
                                        monocarboxylic acid 17476
                                          fatty acid 15990
                                            short-chain fatty acid 15674
                                              fatty acid 4:0 7810
                                                butyric acid 6168
                                                  indole-3-butyric acid 6
                                                    4-(indol-3-yl)butanoyl-beta-D-glucose 0
                                                    N(2)-[4-(indol-3-yl)butanoyl]-L-glutamine 0
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