neohesperidin

Metabolite details

Identifier

ARGKVCXINMKCAZ-UZRWAPQLSA-N

InChI Key

ARGKVCXINMKCAZ-UZRWAPQLSA-N

IUPAC name

(2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(α-L-rhamnopyranosyl)-β-D-glucopyranoside

Preferred name

neohesperidin

INN name

—

Synonym

(S)-7-(((2-O-6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one

ChEBI

CHEBI:59016

Reactome pathways

• No Reactome pathways listed for this metabolite.

Observed in studies

• Jasmonate-mediated stomatal closure under elevated CO2 revealed by time-resolved metabolomics
• Metabolic plasticity confers increased resilience to climate variability in temperate compared to tropical lizards
• Metabolic profilings of rat INS-1 β-cells under changing levels of essential amino acids
• Integrated Metabolomics and Transcriptomics Analyses Reveal Anthocyanin and Carotenoid Biosynthesis Involved in Color Development in Willow Bark
• Multiomic analysis revealed the potential role of rumen microbes in heat stress
• Effect of heat stress on serum enzyme activity, antioxidant capacity and immune parameter metabolomics datasets in Holstein cows at different growth stages
• Extracellular-acidosis restricts one-carbon metabolism and preserves T cell stemness

Observed in differential profiles

• 400ppm_0min_vs_800ppm_60min
• T_septentrionalis_cold_vs_T_septentrionalis_warm
• G1_Control_vs_G2_Arginine_Addition
• Purple_vs_Green
• Dc-N_vs_Dc-HS
• Dcs_N_vs_Dcs_HS
• Control_vs_Lactic_Acid