Structures, targets and recent approaches in anti-leishmanial drug discovery and development.

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2011-01-01 Epub Date: 2011-03-09 DOI:10.2174/1874104501105010031
Karin Seifert
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引用次数: 91

Abstract

Recent years have seen a significant improvement in available treatment options for leishmaniasis. Two new drugs, miltefosine and paromomycin, have been registered for the treatment of visceral leishmaniasis (VL) in India since 2002. Combination therapy is now explored in clinical trials as a new treatment approach for VL to reduce the length of treatment and potentially prevent selection of resistant parasites. However there is still a need for new drugs due to safety, resistance, stability and cost issues with existing therapies. The search for topical treatments for cutaneous leishmaniasis (CL) is ongoing. This review gives a brief overview of recent developments and approaches in anti-leishmanial drug discovery and development.

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抗利什曼原虫药物的结构、靶点和最新研究进展。
近年来,利什曼病的现有治疗方案有了显著改善。自2002年以来,两种新药米特福辛和帕罗霉素已经在印度注册用于治疗内脏利什曼病(VL)。目前,临床试验正在探索联合治疗作为VL的一种新的治疗方法,以缩短治疗时间并可能防止耐药寄生虫的选择。然而,由于现有疗法的安全性、耐药性、稳定性和成本问题,仍然需要新的药物。寻找皮肤利什曼病(CL)的局部治疗方法正在进行中。本文综述了近年来抗利什曼原虫药物的发现和开发的最新进展和方法。
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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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