89859-74-5

Upstream product

• 74766-86-2 DL-3,4-di-O-Acetyl-1,2-anhydro-(1,2,3/4)-5-benzoyloxymethyl-5-cyclohexene-1,2,3,4-tetrol 
• 38231-86-6 valienamine 
• 89859-46-1 methyl 6-O-acetyl-2,3-cyclohexylidene-α-D-xylo-hexopyranosid-4-ulose 
• 4097-95-4 Methyl-4-amino-4-deoxy-α-D-glucopyranoside 
• 141232-09-9 Benzoic acid 4,5,6-triacetoxy-3-((2S,3R,4S,5R,6S)-4,5-diacetoxy-2-acetoxymethyl-6-methoxy-tetrahydro-pyran-3-ylamino)-cyclohex-1-enylmethyl ester 
• 81692-19-5 DL-4,7:5,6-di-O-isopropylidene-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexenylamine 
• 24578-12-9 Methyl 3,4-anhydro-α-D-galactopyranoside 
• 101072-28-0 methyl 2,3,6,4',5',6',7'-hepta-O-acetyl-4-deoxy-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexenylamino>-α-D-glucopyranoside 

Downstream Products

• 101072-28-0 methyl 2,3,6,4',5',6',7'-hepta-O-acetyl-4-deoxy-4-<(1S)-(1,4,6/5)-4,5,6-trihydroxy-3-hydroxymethyl-2-cyclohexenylamino>-α-D-glucopyranoside 

Relevant academic research and scientific papers

Chemical modification of the sugar part of methyl acarviosin: Synthesis and inhibitory activities of nine analogues

Nine analogues of methyl acarviosin (1), the core structure of acarbose and its homologues, the 6-hydroxy-(2), 6-azido-(3), 6-amino-(4), 6-acctamido-(5), 6-methoxy-(6), 6-hydroxy-2-O-methyl-(8), and 6-hydroxy-3-O-methyl derivatives (9), including the 5-me

SYTHESIS OF ADIPOSIN-1 AND RELATED COMPOUNDS

The synthesis is described of adiposin-1 (2a), isolated from an α-D-glucosidase inhibitor complex, adiposin, produced by Streptomyces calvus TM-521.The synthesis involved the coupling of 1,6-anhydro-4-O-(3,4-anhydro-α-D-galactopyranosyl)-β-D-glucopyranose