CHEBI:18743 - (S)-2-trans-abscisic acid

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ChEBI Name (S)-2-trans-abscisic acid
ChEBI ID CHEBI:18743
ChEBI ASCII Name (S)-2-trans-abscisic acid
Definition A 2-trans-abscisic acid with (S)-configuration at the chiral centre.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C15H20O4
Net Charge 0
Average Mass 264.31690
Monoisotopic Mass 264.13616
InChI InChI=1S/C15H20O4/c1-10(7-13(17)18)5-6-15(19)11(2)8-12(16)9-14(15,3)4/h5-8,19H,9H2,1-4H3,(H,17,18)/b6-5+,10-7+/t15-/m1/s1
InChIKey JLIDBLDQVAYHNE-IBPUIESWSA-N
SMILES CC(\C=C\[C@@]1(O)C(C)=CC(=O)CC1(C)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 )
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ChEBI Ontology
Outgoing (S)-2-trans-abscisic acid (CHEBI:18743) is a 2-trans-abscisic acid (CHEBI:62426)
(S)-2-trans-abscisic acid (CHEBI:18743) is conjugate acid of (S)-2-trans-abscisate (CHEBI:62421)
(S)-2-trans-abscisic acid (CHEBI:18743) is enantiomer of (R)-2-trans-abscisic acid (CHEBI:18657)
Incoming (S)-2-trans-abscisic acid β-D-glucopyranosyl ester (CHEBI:62437) has functional parent (S)-2-trans-abscisic acid (CHEBI:18743)
(S)-2-trans-abscisic acid D-glucopyranosyl ester (CHEBI:62438) has functional parent (S)-2-trans-abscisic acid (CHEBI:18743)
(S)-2-trans-abscisate (CHEBI:62421) is conjugate base of (S)-2-trans-abscisic acid (CHEBI:18743)
(R)-2-trans-abscisic acid (CHEBI:18657) is enantiomer of (S)-2-trans-abscisic acid (CHEBI:18743)
IUPAC Name
(2E,4E)-5-[(1S)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid
Synonyms Sources
(7E,9E)-(6S)-6-hydroxy-3-oxo-11-apo-ε-caroten-11-oic acid JCBN
(S)-2-trans-abscisic acid ChEBI
2-trans-(+)-ABA ChEBI
Manual Xref Database
LMPR0103050001 LIPID MAPS
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Registry Number Type Source
3034278 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
12114582 PubMed citation Europe PMC
Last Modified
24 June 2011