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二氢叶酸还原酶抑制剂作为抗菌剂。

Dihydrofolate reductase inhibitors as antibacterial agents.

作者信息

Hawser Stephen, Lociuro Sergio, Islam Khalid

机构信息

Arpida Ltd., Dammstrasse 36, 4142 Münchenstein, Switzerland.

出版信息

Biochem Pharmacol. 2006 Mar 30;71(7):941-8. doi: 10.1016/j.bcp.2005.10.052. Epub 2005 Dec 13.

Abstract

Although only a few DHFR inhibitors have progressed as antibiotics to the market there is much renewed interest in the discovery and development of new generation DHFR inhibitors as antibacterial agents. This article describes the success in exploiting DHFR as a drugable target as exemplified by trimethoprim (TMP) and the development of several new diaminopyrimidines. Iclaprim, a recent example of a novel diaminopyrimidine currently in Phase III clinical trials, is also described together with several examples of anti-DHFR antibacterial compounds in pre-clinical development.

摘要

尽管只有少数二氢叶酸还原酶(DHFR)抑制剂作为抗生素进入市场,但新一代DHFR抑制剂作为抗菌剂的发现和开发重新引起了人们的广泛关注。本文介绍了以甲氧苄啶(TMP)为例,将DHFR作为可成药靶点的成功经验,以及几种新型二氨基嘧啶的开发情况。还介绍了处于III期临床试验阶段的新型二氨基嘧啶类药物依克拉普明,以及临床前开发阶段的几种抗DHFR抗菌化合物。

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