CHEBI:136433 - 2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid
ChEBI ID CHEBI:136433
Definition A member of the class of indoles obtained by dimerisation of 2-imino-3-(indol-3-yl)propanoic acid. An intermediate in the biosynthesis of violacein.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C22H18N4O4
Net Charge 0
Average Mass 402.404
Monoisotopic Mass 402.13281
InChI InChI=1S/C22H18N4O4/c23-19(21(27)28)17(13-9-25-15-7-3-1-5-11(13)15)18(20(24)22(29)30)14-10-26-16-8-4-2-6-12(14)16/h1-10,17-18,23-26H,(H,27,28)(H,29,30)
InChIKey CKBGWXPNAUCVQQ-UHFFFAOYSA-N
SMILES C1=CC=CC2=C1C(=CN2)C(C(C3=CNC=4C3=CC=CC4)C(C(=O)O)=N)C(C(=O)O)=N
Metabolite of Species Details
Chromobacterium violaceum (NCBI:txid536) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) has functional parent 2-imino-3-(indol-3-yl)propanoic acid (CHEBI:90891)
2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) has role bacterial metabolite (CHEBI:76969)
2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) is a dicarboxylic acid (CHEBI:35692)
2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) is a indoles (CHEBI:24828)
2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) is a ketimine (CHEBI:33272)
2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433) is tautomer of 2,5-diiminio-3,4-bis(indol-3-yl)hexanedioate (CHEBI:133928)
Incoming 2,5-diiminio-3,4-bis(indol-3-yl)hexanedioate (CHEBI:133928) is tautomer of 2,5-diimino-3,4-bis(indol-3-yl)hexanedioic acid (CHEBI:136433)
IUPAC Name
2,5-diimino-3,4-di(1H-indol-3-yl)hexanedioic acid
Synonym Source
indole-3-pyruvic acid imine dimer ChEBI
Citations Waiting for Citations Types Sources
17176066 PubMed citation Europe PMC
18171677 PubMed citation Europe PMC
Last Modified
07 March 2017