194980-11-5

Basic information

• Product Name: (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester
• Synonyms: (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester
• CAS NO: 194980-11-5
• Molecular Weight: 1026.36
• Mol File: 194980-11-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester(194980-11-5)
• EPA Substance Registry System: (S)-2-[2-((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetylamino]-pentanedioic acid dibenzyl ester(194980-11-5)

Safety Data

• Hazardous Substances Data: 194980-11-5(Hazardous Substances Data)

Upstream product

• 2791-84-6 L-glutamic acid dibenzyl ester 4-toluenesulfonate 
• 194980-03-5 ((2R,3R,4R,5R,6R)-3,4,5-Tris-benzyloxy-6-hexadecyloxymethyl-tetrahydro-pyran-2-yl)-acetic acid 
• 3879-79-6 (2R,3R,4S,5S,6S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)-6-methoxytetrahydro-2H-pyran 
• 194410-25-8 9-O-acetyl-4,8-anhydro-5,6,7-tri-O-benzyl-1,2,3-trideoxy-D-glycero-D-galacto-non-1-enitol 
• 194980-05-7 3-(6-O-hexadecanyl-2,3,4-tri-O-benzyl-α-D-mannopyranosyl)propene 
• 223263-24-9 ((2R,3R,4R,5R,6R)-6-Allyl-3,4,5-tris-benzyloxy-tetrahydro-pyran-2-yl)-methanol 
• 112-82-3 hexadecanyl bromide 

Relevant articles and documents

Small molecules as structural and functional mimics of sialyl Lewis X tetrasaccharide in selectin inhibition: A remarkable enhancement of inhibition by additional negative charge and/or hydrophobic group

Several sialyl Lewis X (SLe(X))) mimics that contain the essential functional groups for receptor interaction and a negative charge or a hydrophobic group have been developed as inhibitors of E-, P-, and L-selectins. Some of the mimics exhibit selectin in