(2S)-5,7,3',4'-Tetrahydroxyflavanone 7-(6-p-coumaroylglucoside)

Metabolite details

Identifier

OGVBUVNWHBXNFL-UNTJOBKYSA-N

InChI Key

OGVBUVNWHBXNFL-UNTJOBKYSA-N

IUPAC name

[(3S,4S,6S)-6-[[(2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate

Preferred name

(2S)-5,7,3',4'-Tetrahydroxyflavanone 7-(6-p-coumaroylglucoside)

INN name

—

Synonym

—

ChEBI

CHEBI:168019

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Metabolomic Insights into the Browning of the Peel of Bagging ‘Rui Xue’ Apple Fruit
• Integrated Four Comparative-Omics Reveals the Mechanism of the Terpenoid Biosynthesis in Two Different Overwintering <i>Cryptomeria fortunei</i> Phenotypes.
• Transcriptome and metabolome changes in Chinese cedar during cold acclimation reveal the roles of flavonoids in needle discoloration and cold resistance.
• Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon

Observed in differential profiles

• Non_Bagged_Fruits_vs_Bagged_Fruits_With_Browning
• WT_vs_GM
• Wild_Type_vs_Evergreen_Mutant
• Male_19_days_vs_Male_1_day