New chiral stationary phase with macrocyclic glycopeptide Z-D antibiotic eremomycin chemically bonded to silica

被引:50
作者
Staroverov, SM
Kuznetsov, MA
Nesterenko, PN
Vasiarov, GG
Katrukha, GS
Fedorova, GB
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119992, Russia
[2] JSC BioChemMack S&T, Moscow 119992, Russia
[3] Russian Acad Med Sci, Gause Inst New Antibiot, Moscow 119021, Russia
关键词
eremomycin; ristocetin A; vancomycin; macrocyclic glycopeptide antibiotics; enantiomeric separations; chiral stationary phases; amino acids;
D O I
10.1016/j.chroma.2006.01.073
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new chiral stationary phase (CSP) was prepared by attachment of rnacrocyclic glycopeptide antibiotic eremomycin to the epoxy-activated silica under mild conditions. In contrast to CSP with immobilized vancomycin, which is a close structural analogue of eremomycin, the prepared CSP reveals high enantioselectivity for separation of amino acids enantiorners. It was demonstrated by the example of ristocetin A CSP that method of the immobilization of macrocyclic glycopeptide antibiotics affects remarkably the resulting enantioselectivity. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:263 / 267
页数:5
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