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

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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

Download	Molfile XML SDF

Formula

C15H20O4

Net Charge

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 )

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

Registry Number	Type	Source
3034278	Reaxys Registry Number	Reaxys

Citation	Type	Source
12114582	PubMed citation	Europe PMC

Last Modified

24 June 2011