๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis of E-selectin inhibitors: Use of an aryl-cyclohexyl ether as a disaccharide scaffold

โœ Scribed by Aijun Liu; Kathleen Dillon; Robert M. Campbell; Don C. Cox; Donna M. Huryn

Book ID
103406004
Publisher
Elsevier Science
Year
1996
Tongue
French
Weight
235 KB
Volume
37
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Enzymatic synthesis of a sialyl Lewis X
Enzymatic synthesis of a sialyl Lewis X dimer from egg yolk as an inhibitor of E-selectin
โœ Chun-Hung Lin; Makoto Shimazaki; Chi-Huey Wong; Mamoru Koketsu; Lekh Raj Juneja; ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 385 KB

A dimeric sialyl Lewis X (SLex) glycopeptide was synthesized enzymatically in three steps from an N-linked oligosaccharide prepared from egg yolk. Treatment of delipidated hen egg yolk with the protease Orientase and neuraminidase gave a dimeric N-acetyllactosamine-containing oligosaccharide linked

New EPSP synthase inhibitors: Synthesis
New EPSP synthase inhibitors: Synthesis and evaluation of an aromatic tetrahedral intermediate mimic containing a 3-malonate ether as a 3-phosphate surrogate
โœ Michael J. Miller; Darryl G. Cleary; Joel E. Ream; Kristin R. Snyder; James A. S ๐Ÿ“‚ Article ๐Ÿ“… 1995 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 719 KB

A new analog of the EPSP synthase enzyme reaction intermediate 1, containing a 3-malonate ether moiety in place of the usual 3-phosphate group, was synthesized from 3,5-dihydroxybenzoic acid. This simple, synthetically accessible aromatic compound (5) is an effective competitive inhibitor versus S3P