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

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

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 Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search 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 ) View more via ChEBI Ontology 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 View more database links Registry Numbers Types Sources 3034278 Reaxys Registry Number Reaxys 3034278 Beilstein Registry Number Beilstein Citation Type Source 12114582 PubMed citation Europe PMC Last Modified 24 June 2011