89616-07-9

Basic information

• Product Name: (4S)-α-terpineol 8-O-β-D-glucopyranoside
• Synonyms: (4S)-α-terpineol 8-O-β-D-glucopyranoside
• CAS NO: 89616-07-9
• Molecular Weight: 316.395
• Mol File: 89616-07-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4S)-α-terpineol 8-O-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-α-terpineol 8-O-β-D-glucopyranoside(89616-07-9)
• EPA Substance Registry System: (4S)-α-terpineol 8-O-β-D-glucopyranoside(89616-07-9)

Safety Data

• Hazardous Substances Data: 89616-07-9(Hazardous Substances Data)

Upstream product

• 918803-49-3 (4S)-α-terpineol 8-O-β-D-(3'-O,4'-O,6'-O-triacetyl)glucopyranoside 
• 10482-56-1 (-)-(S)-α-terpineol 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 

Downstream Products

• 10482-56-1 (-)-(S)-α-terpineol 

Relevant articles and documents

Cacalol derivatives from Roldana angulifolia

Four new modified eremophilanes, angulifolide (1) and angulifolins A-C (2-4), and two new triacetylglucosides (7 and 8) were isolated from Roldana angulifolia, together with several known compounds. The structures of the new compounds were elucidated by spectroscopic analysis and chemical reactions. The absolute configuration of compounds 2 and 3 was established by Mosher ester methodology. Cytotoxicity against selected human cancer cell lines was determined for the more abundant isolated metabolites.

Inhibitory effects of perillosides A and C, and related monoterpene glucosides on aldose reductase and their structure-activity relationships.

Monoterpene glucosides, perillosides A and C, obtained from the leaves of Perilla frutescens, were found to be inhibitors of aldose reductase (EC 1.1.1.21) which is considered to be a key enzyme in diabetic complications such as cataract. The apparent typ