Lipase-Catalyzed Kinetic Resolution of Novel Antifungal N-Substituted Benzimidazole Derivatives

被引:7
|
作者
Lukowska-Chojnacka, Edyta [1 ]
Staniszewska, Monika [2 ]
Bondaryk, Malgorzata [2 ]
Maurin, Jan K. [3 ,4 ]
Bretner, Maria [1 ]
机构
[1] Warsaw Univ Technol, Fac Chem, Inst Biotechnol, Noakowskiego St 3, PL-00664 Warsaw, Poland
[2] Natl Inst Publ Hlth Natl Inst Hyg, Independent Lab Streptomyces & Fungi Imperfecti, Warsaw, Poland
[3] Natl Ctr Nucl Res, PL-05400 Otwock, Poland
[4] Natl Med Inst, Warsaw, Poland
关键词
azole; benzimidazole; enzyme; lipase; enzymatic transesterification; kinetic resolution; antifungal activity; CHEMOENZYMATIC SYNTHESIS; ESTERS;
D O I
10.1002/chir.22591
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of new N-substituted benzimidazole derivatives was synthesized and their antifungal activity against Candida albicans was evaluated. The chemical step included synthesis of appropriate ketones containing benzimidazole ring, reduction of ketones to the racemic alcohols, and acetylation of alcohols to the esters. All benzimidazole derivatives were obtained with satisfactory yields and in relatively short times. All synthesized compounds exhibit significant antifungal activity against Candida albicans 900028 ATCC (% cell inhibition at 0.25g concentration>98%). Additionally, racemic mixtures of alcohols were separated by lipase-catalyzed kinetic resolution. In the enzymatic step a transesterification reaction was applied and the influence of a lipase type and solvent on the enantioselectivity of the reaction was studied. The most selective enzymes were Novozyme SP 435 and lipase Amano AK from Pseudomonas fluorescens (E>100). Chirality 28:347-354, 2016. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:347 / 354
页数:8
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