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CHEBI:32903 - gibberellin A7

Default Structure
ChEBI IDCHEBI:32903
ChEBI Namegibberellin A7
Stars
ASCII Namegibberellin A7
DefinitionA C19-gibberellin that is a pentacyclic diterpenoid responsible for promoting growth and development in plants. Initially identified in Gibberella fujikuroi, it differs from gibberellin A1 in lacking the OH at C-7 (gibbane numbering).
Secondary ChEBI IDsCHEBI:24248, CHEBI:29603
Last Modified5 September 2018
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC19H22O5
Net Charge0
Average Mass330.380
Monoisotopic Mass330.14672
SMILES[H][C@@]12CC[C@@H]3C[C@]1(CC3=C)[C@@H](C(=O)O)[C@@]1([H])[C@@]23C=C[C@H](O)[C@@]1(C)C(=O)O3
InChIInChI=1S/C19H22O5/c1-9-7-18-8-10(9)3-4-11(18)19-6-5-12(20)17(2,16(23)24-19)14(19)13(18)15(21)22/h5-6,10-14,20H,1,3-4,7-8H2,2H3,(H,21,22)/t10-,11-,12+,13-,14-,17-,18+,19-/m1/s1
InChIKeySEEGHKWOBVVBTQ-NFMPGMCNSA-N
Species of MetaboliteComponentSourceComments
Gibberella fujikuroi (ncbitaxon:5127) - PubMed (24232845)
Leifsonia soli (ncbitaxon:582665) - PubMed (24569847)
Mus musculus (ncbitaxon:10090) - PubMed (19425150) Source: BioModels - MODEL1507180067
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 Roles:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
mouse metabolite  Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
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 A7 (CHEBI:32903) has role bacterial metabolite (CHEBI:76969)
gibberellin A7 (CHEBI:32903) has role mouse metabolite (CHEBI:75771)
gibberellin A7 (CHEBI:32903) has role plant metabolite (CHEBI:76924)
gibberellin A7 (CHEBI:32903) is a C19-gibberellin (CHEBI:20858)
gibberellin A7 (CHEBI:32903) is a gibberellin monocarboxylic acid (CHEBI:38305)
gibberellin A7 (CHEBI:32903) is a lactone (CHEBI:25000)
IUPAC Names 
(1R,2R,5R,8R,9S,10R,11S,12S)-12-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadec-13-ene-9-carboxylic acid
(1S,2S,4aR,4bR,7R,9aR,10S,10aR)-2-hydroxy-1-methyl-8-methylidene-13-oxo-1,2,4b,5,6,7,8,9,10,10a-decahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid
2β-hydroxy-1β-methyl-8-methylidene-13-oxo-4a,1α-epoxymethano-4aα,4bβ-gibb-3-ene-10β-carboxylic acid
Synonyms  Source
(1α,2β,4aα,4bβ,10β)-2,4a-dihydroxy-1-methyl-8-methylenegibb-3-ene-1,10-dicarboxylic acid 1,4a-lactoneChemIDplus
GA7ChEBI
gibberellin 7ChEBI
Gibberellin A7KEGG COMPOUND
Manual XrefsDatabases
C00000007KNApSAcK
C11867KEGG COMPOUND
LMPR0104170024LIPID MAPS
Registry NumbersSources
Beilstein:1439710Beilstein
Beilstein:8359138Beilstein
CAS:510-75-8ChemIDplus
CAS:510-75-8KEGG COMPOUND
Citations