(R)-2-trans-abscisic acid

Metabolite details

Identifier

JLIDBLDQVAYHNE-XQFZKXHBSA-N

InChI Key

JLIDBLDQVAYHNE-XQFZKXHBSA-N

IUPAC name

(2E,4E)-5-[(1R)-1-hydroxy-2,6,6-trimethyl-4-oxocyclohex-2-en-1-yl]-3-methylpenta-2,4-dienoic acid

Preferred name

(R)-2-trans-abscisic acid

INN name

—

Synonym

(7E,9E)-(6R)-6-hydroxy-3-oxo-11-apo-ε-caroten-11-oic acid

ChEBI

CHEBI:18657

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
• Metabolomic Insights into the Browning of the Peel of Bagging ‘Rui Xue’ Apple Fruit
• Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
• Diallyl disulfide (DADS) ameliorates intestinal Candida albicans infection by modulating the gut microbiota and metabolites and providing intestinal protection in mice
• Transcriptome and Metabolome Analyses Reveal Differences in Terpenoid and Flavonoid Biosynthesis in Cryptomeria fortunei Needles Across Different Seasons

Observed in differential profiles

• G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
• Non_Bagged_Fruits_vs_Bagged_Fruits_With_Browning
• Control_vs_nsPEF_7_day
• G1_PBS_vs_G2_DSS
• Summer_vs_Winter