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具有抑制氯喹耐药转运蛋白功能的双功能抗疟药。

Dual-functioning antimalarials that inhibit the chloroquine-resistance transporter.

机构信息

Department of Chemistry, University of Cape Town, Private Bag, Rondebosch 7701, South Africa.

出版信息

Future Microbiol. 2013 Apr;8(4):475-89. doi: 10.2217/fmb.13.18.

Abstract

Malaria remains a major international health challenge. Resistance to a number of existing drugs and evidence of the emergence of artemisinin resistance has emphasized the need for new antimalarials. A new approach has been the preparation of dual-function compounds that include a chloroquine-like antimalarial group and a group that resembles a chloroquine chemosensitizer. This article reviews the recent discovery of such dual-function antimalarials that are proposed to target both hemozoin formation and the chloroquine resistance transporter, PfCRT. These are discussed in relation to the mechanism of action of 4-aminoquinolines, chloroquine resistance and resistance reversal.

摘要

疟疾仍然是一个重大的国际健康挑战。对一些现有药物的耐药性以及青蒿素耐药性出现的证据强调了需要新的抗疟药物。一种新的方法是制备具有双重功能的化合物,其中包括氯喹样抗疟药基团和类似于氯喹化学增敏剂的基团。本文综述了最近发现的这种双重功能的抗疟药物,它们被认为可以靶向疟原虫血红素形成和氯喹耐药转运蛋白 PfCRT。这些药物的作用机制、4-氨基喹啉类药物的耐药性和耐药逆转等方面进行了讨论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bda/7099626/f52e5fc36ed3/fmb-08-475-g1.jpg

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