myricetin 3-O-β-D-galactopyranoside

Metabolite details

Identifier

FOHXFLPXBUAOJM-MGMURXEASA-N

InChI Key

FOHXFLPXBUAOJM-MGMURXEASA-N

IUPAC name

5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl β-D-galactopyranoside

Preferred name

myricetin 3-O-β-D-galactopyranoside

INN name

—

Synonym

myricetin-3-O-β-D-galactoside

ChEBI

CHEBI:75815

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Multi-Omics Analysis Reveals Disturbance of Nanosecond Pulsed Electric Field in the Serum Metabolic Spectrum and Gut Microbiota
• Chromosome‐level genome of
• Characterization of white tea metabolome: comparison against green and black tea by a nontargeted metabolomics approach.
• Phosphoproteomic and Metabolomic Profiling Uncovers the Roles of CcPmk1 in the Pathogenicity of <i>Cytospora chrysosperma</i>
• Integrated Metabolomics and Transcriptomics Analyses Reveal Anthocyanin and Carotenoid Biosynthesis Involved in Color Development in Willow Bark
• Comprehensive analysis of metabolome and transcriptome reveals the mechanism of color formation in different leave of Loropetalum chinense var. rubrum

Observed in differential profiles

• Control_vs_nsPEF_7_day
• Flower_vs_Kernel
• White_Tea_0h_vs_White_Tea_36h
• CcPmk1_vs_Wild_type
• Purple_vs_Green
• Green_Leaf_vs_Purple_Leaf