1383450-25-6

Basic information

• Product Name: 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol
• Synonyms: 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol
• CAS NO: 1383450-25-6
• Molecular Weight: 649.738
• Mol File: 1383450-25-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol(1383450-25-6)
• EPA Substance Registry System: 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol(1383450-25-6)

Safety Data

• Hazardous Substances Data: 1383450-25-6(Hazardous Substances Data)

Upstream product

• 479252-05-6 ((2R,3R,4S,5R,6S)-3,4,5-Tris-benzyloxy-6-p-tolylsulfanyl-tetrahydro-pyran-2-yl)-methanol 
• 1383450-17-6 1,2-di-O-hydrocinnamoyl-3-O-(N-hydrocinnamoyl-6'-amino-2',3',4'-tri-O-benzyl-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol 
• 1383449-95-3 p-tolyl 2,3,4-tri-O-benzyl-6-O-p-tosyl-1-thio-β-D-glucopyranoside 
• 1383450-05-2 3-O-(6'-amino-2',3',4'-tri-O-benzyl-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol 
• 1383449-98-6 6-azido-2,3,4-tri-O-benzyl-6-deoxy-α-D-glucopyranosyl trichloroacetimidate 
• 1192755-04-6 3-O-(6'-azido-2',3',4'-tri-O-benzyl-6'-deoxy-α-D-glucopyranosyl)-sn-glycerol 
• 1192755-03-5 3-O-(6'-azido-2',3',4'-tri-O-benzyl-6'-deoxy-α-D-glucopyranosyl)-1,2-O-isopropylidene-sn-glycerol 

Relevant articles and documents

Synthesis of glycoglycerolipid of 1,2-dipalmitoyl-3-(N-palmitoyl-6′- amino-6′-deoxy-α-D-glucosyl)-sn-glycerol and its analogues, inhibitors of human Myt1-kinase

A glycoglycerolipid 1a isolated from a marine alga showed inhibition to Myt1 kinase with IC50 of 0.12 μg/mL. We synthesized 1a and its seven analogues (1b-h) in an efficient method with high stereoselectivity. The process employed trichloroacetimidate donor 4b at low substrate concentration to achieve high α-selectivity (α/β = 33:1) in glycosylation reaction. The present synthesis provided various acyl derivatives required for the study on the structure-activity relationship later.