Novel compounds active against Leishmania major.

Novel compounds active against Leishmania major.
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新型化合物对利什曼原虫具有活性。

DOI:
10.1128/aac.50.2.474-479.2006
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发表时间:
2006
期刊:
Antimicrobial agents and chemotherapy.
影响因子:
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通讯作者:
Selitrennikoff,ClaudeP
Selitrennikoff,ClaudeP
中科院分区:
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文献类型:
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作者:
StGeorge,Stephanie;Bishop,JeanetteV;Titus,RichardG;Selitrennikoff,ClaudeP

文献摘要

相似文献

主要利什曼原虫是一种重要的锥虫病原体,导致利什曼病,这是一种严重的疾病,在许多旧世界。目前的治疗方法包括少量的锑化合物,虽然有些有效,但受到严重副作用的限制。我们已经筛选了一个独特的化学库的一小部分,并发现了至少三个新的化合物,是有效的。tarentolaeandL.主要在体外和小鼠巨噬细胞模型中的L.严重感染这些化合物在显著低于葡萄糖酸锑钠(Pentoclavine)的剂量下在两种测定中均有效,代表了药物开发的可能候选物。
Leishmania majoris an important trypanosomatid pathogen that causes leishmaniasis, which is a serious disease in much of the Old World. Current treatments include a small number of antimony compounds that, while somewhat effective, are limited by serious side effects. We have screened a small portion of a unique chemical library and have found at least three novel compounds that are effective againstL. tarentolaeandL. majorin vitro and in a murine macrophage model ofL. majorinfection. These compounds were effective in both assays at doses significantly lower than those of sodium stibogluconate (Pentostam) and represent possible candidates for drug development.