CHEBI:545687 - traumatic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name traumatic acid
ChEBI ID CHEBI:545687
Definition A monounsaturated straight-chain dicarboxylic acid with the double bond at C-2; a plant wound-healing hormone.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C12H20O4
Net Charge 0
Average Mass 228.28480
Monoisotopic Mass 228.13616
InChI InChI=1S/C12H20O4/c13-11(14)9-7-5-3-1-2-4-6-8-10-12(15)16/h7,9H,1-6,8,10H2,(H,13,14)(H,15,16)/b9-7+
InChIKey MAZWDMBCPDUFDJ-VQHVLOKHSA-N
SMILES OC(=O)CCCCCCCC\C=C\C(O)=O
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): plant hormone
A plant growth regulator that modulates the formation of stems, leaves and flowers, as well as the development and ripening of fruit. The term includes endogenous and non-endogenous compounds (e.g. active compounds produced by bacteria on the leaf surface) as well as semi-synthetic and fully synthetic compounds.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing traumatic acid (CHEBI:545687) has role plant hormone (CHEBI:37848)
traumatic acid (CHEBI:545687) is a dicarboxylic acid (CHEBI:35692)
Incoming trans-2-dodecenedioyl-CoA (CHEBI:76427) has functional parent traumatic acid (CHEBI:545687)
IUPAC Name
(2E)-dodec-2-enedioic acid
Synonyms Sources
(2E)-Dodecenedioic acid KEGG COMPOUND
2E-dodecenedioic acid LIPID MAPS
Dodec-2-enedioic acid ChemIDplus
Dodec-2-enedioic acid KEGG COMPOUND
trans-2-dodecenedioic acid LIPID MAPS
Manual Xrefs Databases
C16308 KEGG COMPOUND
LMFA01170002 LIPID MAPS
View more database links
Registry Numbers Types Sources
1725762 Beilstein Registry Number Beilstein
6402-36-4 CAS Registry Number KEGG COMPOUND
6402-36-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11978597 PubMed citation Europe PMC
16588378 PubMed citation Europe PMC
17791417 PubMed citation Europe PMC
Last Modified
23 October 2015