Urs-12-en-28-oic acid, 3-(α-L-arabinopyranosyloxy)-23-hydroxy-, O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, (3β,4α)- (9CI) is a complex triterpenoid glycoside characterized by its unique structural features, including a ursane-type skeleton and multiple sugar moieties. The presence of the ursane backbone suggests potential biological activities, as triterpenoids are known for their anti-inflammatory, antioxidant, and anticancer properties. The glycosidic linkages involving arabinose and glucose units indicate that this compound may exhibit enhanced solubility and bioavailability compared to its aglycone counterparts. Its stereochemistry, particularly at the 3β and 4α positions, contributes to its specific interactions with biological targets. The compound's CAS number, 160669-29-4, facilitates its identification in chemical databases, aiding in research and application in fields such as pharmacology and natural product chemistry. Overall, this substance represents a significant area of interest for further investigation into its potential therapeutic effects and mechanisms of action.

Urs-12-en-28-oic acid,3-(a-L-arabinopyranosyloxy)-23-hydroxy-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)- (9CI)

160669-29-4: Urs-12-en-28-oic acid, 3-(α-L-arabinopyranosyloxy)-23-hydroxy-, O-6-deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, (3β,4α)- (9CI) is a complex triterpenoid glycoside characterized by its unique structural features, including a ursane-type skeleton and multiple sugar moieties. The presence of the ursane backbone suggests potential biological activities, as triterpenoids are known for their anti-inflammatory, antioxidant, and anticancer properties. The glycosidic linkages involving arabinose and glucose units indicate that this compound may exhibit enhanced solubility and bioavailability compared to its aglycone counterparts. Its stereochemistry, particularly at the 3β and 4α positions, contributes to its specific interactions with biological targets. The compound's CAS number, 160669-29-4, facilitates its identification in chemical databases, aiding in research and application in fields such as pharmacology and natural product chemistry. Overall, this substance represents a significant area of interest for further investigation into its potential therapeutic effects and mechanisms of action.

<p>Scheffursoside C is a useful organic compound for research related to life sciences. The catalog number is T125696 and the CAS number is 160669-29-4.</p>

CAS 160669-29-4

Urs-12-en-28-oic acid,3-(a-L-arabinopyranosyloxy)-23-hydroxy-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)- (9CI)

Scheffursoside C

Ref: TM-T125696