首页> 外文期刊>The Open Medicinal Chemistry Journal >Structures, Targets and Recent Approaches in Anti-Leishmanial Drug Discovery and Development
【24h】

Structures, Targets and Recent Approaches in Anti-Leishmanial Drug Discovery and Development

机译:反利什曼药物发现和开发的结构,目标和最新方法

获取原文
           

摘要

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.
机译:近年来,在利什曼病的可用治疗选择中已取得了显着改善。自2002年以来,印度已经注册了两种新药miltefosine和paromomycin用于内脏利什曼病(VL)的治疗。现在,临床试验中正在探索组合疗法作为VL的新治疗方法,以缩短治疗时间并可能防止选择抗性寄生虫。然而,由于现有疗法的安全性,耐药性,稳定性和成本问题,仍然需要新药。皮肤利什曼病(CL)的局部治疗的研究正在进行中。这篇综述简要概述了抗利什曼病药物发现和开发的最新发展和方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号