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布雷喹那衍生物与二氢乳清酸脱氢酶的物种特异性药物设计

Brequinar derivatives and species-specific drug design for dihydroorotate dehydrogenase.

作者信息

Hurt Darrell E, Sutton Amanda E, Clardy Jon

机构信息

Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14850, USA.

出版信息

Bioorg Med Chem Lett. 2006 Mar 15;16(6):1610-5. doi: 10.1016/j.bmcl.2005.12.029. Epub 2006 Jan 10.

Abstract

Therapeutic agents brequinar sodium and leflunomide (Arava) work by binding in a hydrophobic tunnel formed by a highly variable N-terminus of family 2 dihydroorotate dehydrogenase (DHODH). The X-ray crystallographic structure of an analog of brequinar bound to human DHODH was determined. In silico screening of a library of compounds suggested another subset of brequinar analogs that do not inhibit human DHODH as potentially effective inhibitors of Plasmodium falciparum DHODH.

摘要

治疗药物布喹那钠和来氟米特(爱若华)通过结合在由2型二氢乳清酸脱氢酶(DHODH)高度可变的N端形成的疏水通道中发挥作用。测定了与人类DHODH结合的布喹那类似物的X射线晶体结构。对化合物库的计算机筛选表明,另一组不抑制人类DHODH的布喹那类似物可能是恶性疟原虫DHODH的有效抑制剂。

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