CHEBI:29589 - gibberellin A14 aldehyde

ChEBI IDCHEBI:29589
ChEBI Namegibberellin A14 aldehyde
Stars
ASCII Namegibberellin A14 aldehyde
DefinitionA C20-gibberellin obtained by selective reduction of the 10β-carboxy group of gibberellin A14.
Last Modified28 July 2014
DownloadsMolfile
FormulaC20H28O4
Net Charge0
Average Mass332.440
Monoisotopic Mass332.19876
SMILES[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C=O)[C@@]1([H])[C@@]2(C)CC[C@H](O)[C@@]1(C)C(=O)O
InChIInChI=1S/C20H28O4/c1-11-8-20-9-12(11)4-5-14(20)18(2)7-6-15(22)19(3,17(23)24)16(18)13(20)10-21/h10,12-16,22H,1,4-9H2,2-3H3,(H,23,24)/t12-,13+,14+,15+,16+,18+,19-,20-/m1/s1
InChIKeyYMDYUWHAQBYOMU-HYAYUQHRSA-N
Roles Classification
Chemical Roles:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Role:
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.
ChEBI Ontology
Outgoing Relation(s)
gibberellin A14 aldehyde (CHEBI:29589) has functional parent gibberellin A14 (CHEBI:29588)
gibberellin A14 aldehyde (CHEBI:29589) is a C20-gibberellin (CHEBI:20859)
gibberellin A14 aldehyde (CHEBI:29589) is a gibberellin monocarboxylic acid (CHEBI:38305)
gibberellin A14 aldehyde (CHEBI:29589) is conjugate acid of gibberellin A14 aldehyde(1−) (CHEBI:143960)
Incoming Relation(s)
gibberellin A14 aldehyde(1−) (CHEBI:143960) is conjugate base of gibberellin A14 aldehyde (CHEBI:29589)
IUPAC Names 
(1R,2S,3S,4S,5S,8S,9S,12R)-2-formyl-5-hydroxy-4,8-dimethyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-4-carboxylic acid
10β-formyl-2β-hydroxy-1β,4a-dimethyl-8-methylidene-4aα,4bβ-gibbane-1α-carboxylic acid
Synonym  Source
Gibberellin A14 aldehydeKEGG COMPOUND
Manual XrefsDatabases
C11853KEGG COMPOUND
LMPR0104170010LIPID MAPS
C00007331KNApSAcK
Registry NumbersSources
Reaxys:2706728Reaxys
CAS:35470-76-9KEGG COMPOUND