Hebevinoside IV

(2S,3R,4S,5R)-2-[[(7R,9R,10R,13R,14S,16R,17R)-16-hydroxy-7-methoxy-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-3-yl]oxy]oxane-3,4,5-triol

AKDNVAKNWZMAKY-ILFBRDFMSA-N CHEBI:172771 0 Reactome links 2 studies

Metabolite details

Identifier: AKDNVAKNWZMAKY-ILFBRDFMSA-N
InChI Key: AKDNVAKNWZMAKY-ILFBRDFMSA-N
IUPAC name: (2S,3R,4S,5R)-2-[[(7R,9R,10R,13R,14S,16R,17R)-16-hydroxy-7-methoxy-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-3-yl]oxy]oxane-3,4,5-triol
Preferred name: Hebevinoside IV
INN name: —
Synonym: —
ChEBI: CHEBI:172771

Reactome pathways

No Reactome pathways listed for this metabolite.

Observed in studies

Metabolic Dynamics of In Vitro CD8+ T Cell Activation.
Transcriptomic dynamics control rapid transition of core crop functions in 'lactating' pigeon

Observed in differential profiles

G3_Experimental_Sample_0h_vs_G11_Experimental_Sample_96h
Male_19_days_vs_Male_1_day