Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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
go back to main search page
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


show annotations for term's descendants           Sort by:
 
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 chr12:19,407,359...19,413,713
Ensembl chr12:19,407,360...19,413,651
JBrowse link
G Ada adenosine deaminase decreases activity EXP indolebutyric acid results in decreased activity of ADA protein CTD PMID:19442822 NCBI chr 3:152,398,745...152,422,854
Ensembl chr 3:152,398,747...152,447,088
JBrowse link
G Bche butyrylcholinesterase decreases activity EXP indolebutyric acid results in decreased activity of BCHE protein CTD PMID:19442822 NCBI chr 2:158,308,674...158,401,148
Ensembl chr 2:158,307,584...158,401,148
JBrowse link
G Mpo myeloperoxidase increases activity EXP indolebutyric acid results in increased activity of MPO protein CTD PMID:19442822 NCBI chr10:72,594,458...72,608,862
Ensembl chr10:72,594,661...72,604,819
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 6:72,858,713...72,861,941
Ensembl chr 6:72,858,712...72,861,941
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 chr13:92,307,593...92,339,406
Ensembl chr13:92,307,586...92,339,404
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19821
    role 19769
      biological role 19769
        molecular messenger 18316
          hormone 18081
            plant hormone 4934
              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 19821
    subatomic particle 19819
      composite particle 19819
        hadron 19819
          baryon 19819
            nucleon 19819
              atomic nucleus 19819
                atom 19819
                  main group element atom 19716
                    p-block element atom 19716
                      carbon group element atom 19640
                        carbon atom 19630
                          organic molecular entity 19630
                            organic group 18737
                              organic divalent group 18728
                                organodiyl group 18728
                                  carbonyl group 18675
                                    carbonyl compound 18675
                                      carboxylic acid 18373
                                        monocarboxylic acid 17636
                                          fatty acid 16008
                                            short-chain fatty acid 15696
                                              fatty acid 4:0 7891
                                                butyric acid 6262
                                                  indole-3-butyric acid 6
                                                    4-(indol-3-yl)butanoyl-beta-D-glucose 0
                                                    N(2)-[4-(indol-3-yl)butanoyl]-L-glutamine 0
paths to the root