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Synthesis of sialyl Lewis x mimetics as selectin inhibitors by enzymatic aldol condensation reactions
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Synthesis of sialyl Lewis x mimetics as selectin inhibitors by enzymatic aldol condensation reactions

Chun-Cheng Lin, Francisco Morís-Varas, Gabriel Weitz-SchmidtChi-Huey Wong
Bioorganic and Medicinal Chemistry, 卷.7(3), 頁碼.425-433
03/1999
PMID: 10220028

摘要

Biochemistry Molecular Medicine Molecular Biology Pharmaceutical Science Drug Discovery Clinical Biochemistry Organic Chemistry
Several D-mannosyl phosphate/phosphonate derivatives have been enzymatically prepared as sialyl Lewis x tetrasaccharide mimics, which showed strong-to-moderate inhibition against E-, P-, and L-selectins. The synthesis of these mimics is very straightforward; mannosyl aldehyde derivatives are condensed with dihydroxyacetone phosphate (DHAP) in the presence of a DHAP-dependent aldolase to provide mannosyl phosphates. Copyright (C) 1999 Elsevier Science Ltd.

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