The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewis(x)
The design and synthesis of a series of analogues of sialyl Lewis(x)(1) which incorporate conformationally rigid tetralin and naphthalene ring systems(2-4) has led to novel compounds which have similar potency to 1 as inhibitors of cell adhesion.
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Veröffentlicht in: | Bioorganic & medicinal chemistry 1998-12, Vol.6 (12), p.2421-2439 |
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container_title | Bioorganic & medicinal chemistry |
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creator | Murphy, P V Hubbard, R E Manallack, D T Wills, R E Montana, J G Taylor, R J |
description | The design and synthesis of a series of analogues of sialyl Lewis(x)(1) which incorporate conformationally rigid tetralin and naphthalene ring systems(2-4) has led to novel compounds which have similar potency to 1 as inhibitors of cell adhesion. |
doi_str_mv | 10.1016/S0968-0896(98)80017-5 |
format | Article |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Carbohydrate Conformation Carbohydrate Sequence Cell Adhesion - drug effects Cell Adhesion - physiology Cells, Cultured Computer Graphics Drug Design Endothelium, Vascular - cytology Endothelium, Vascular - drug effects Endothelium, Vascular - physiology Fucose HL-60 Cells Humans Indicators and Reagents Models, Molecular Molecular Sequence Data Molecular Structure Naphthalenes Oligosaccharides - chemical synthesis Oligosaccharides - chemistry Oligosaccharides - pharmacology Structure-Activity Relationship Tetrahydronaphthalenes Tumor Necrosis Factor-alpha - pharmacology Umbilical Veins |
title | The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewis(x) |
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