Hebevinoside II

[(2R,3S,4S,5R,6R)-6-[[(7R,9S,10R,13R,14S,16S,17R)-3-[(2S,3R,4R,5R)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-7-hydroxy-4,4,9,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate

RKJPAJOYCCHXQX-OLZOPSFVSA-N CHEBI:185993 0 Reactome links 1 studies

Metabolite details

Identifier: RKJPAJOYCCHXQX-OLZOPSFVSA-N
InChI Key: RKJPAJOYCCHXQX-OLZOPSFVSA-N
IUPAC name: [(2R,3S,4S,5R,6R)-6-[[(7R,9S,10R,13R,14S,16S,17R)-3-[(2S,3R,4R,5R)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-7-hydroxy-4,4,9,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate
Preferred name: Hebevinoside II
INN name: —
Synonym: —
ChEBI: CHEBI:185993

Reactome pathways

No Reactome pathways listed for this metabolite.

Observed in studies

Diallyl disulfide (DADS) ameliorates intestinal Candida albicans infection by modulating the gut microbiota and metabolites and providing intestinal protection in mice

Observed in differential profiles

G1_PBS_vs_G2_DSS