首页> 外文期刊>Current medicinal chemistry. Anti-infective agents >Chitin Synthase As an Antifungal Target: Recent Advances
【24h】

Chitin Synthase As an Antifungal Target: Recent Advances

机译:几丁质合酶作为抗真菌靶标:最新进展

获取原文
获取原文并翻译 | 示例
       

摘要

Chitin is one of the most abundant polysaccharide in the biosphere and consists of unbranched chains of beta-(l,4)-linked 2-acetamido-2-deoxy-D-gIucose units. In yeast and fungi, chitin serves as mechanical support and useful protective barrier for cell walls Since chitin is absent from vertebrates, inhibition of its biosynthesis has been considered as a safe and largely selective therapeutic option. Formation of chitin and its deposition is a highly complex and interconnected series of biochemical and biophysical events and the last step of this biosynthesis is governed by an enzymatic activity called chitin synthase or chitin synthetase The best known and most effective inhibitors of chitin synthase, with marked antifungal activities, are the naturally occurring Polyoxins and Nikkomycins.Extensive efforts have recently been made to look for new naturally occurring CS inhibitors or to modify the basic structure of the existing ones, to improve their inhibitory potencies and their antifungal properties The putative mechanism postulated for the enzymatic process has also been exploited in the design of a new generation of transition-state- or bisubstrate-analogue inhibitors of CS, providing a rational approach in the search for new antifungal agents.
机译:几丁质是生物圈中最丰富的多糖之一,由β-(1,4)-连接的2-乙酰氨基-2-脱氧-D-葡萄糖分子的直链组成。在酵母和真菌中,几丁质可作为机械支持和细胞壁的有用保护屏障。由于脊椎动物不存在几丁质,因此抑制其生物合成已被认为是一种安全且具有选择性的治疗选择。几丁质的形成及其沉积是一系列高度复杂和相互联系的生化和生物物理事件,此生物合成的最后一步是由一种称为几丁质合酶或几丁质合酶的酶活性控制的。几丁质合酶的最著名和最有效的抑制剂,具有抗真菌活性是天然存在的多恶英和尼克霉素。最近人们进行了广泛的努力以寻找新的天然CS抑制剂或改变现有抑制剂的基本结构,以提高其抑制效力和抗真菌性能。在设计新一代CS的过渡态或双底物类似物抑制剂时,还利用了酶促过程,为寻找新的抗真菌剂提供了一种合理的方法。

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