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一个用于发现新型类抗生素的平台
Ian B Seiple1, Ziyang Zhang1, Pavol Jakubec1
1Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, USA.
Nature
|May 20, 2016
概括
一种全合成的新途径使得新型的宏抗生素候选物,包括索利胺,能够产生. 这种方法克服了细菌耐药性,为发现和制造新抗生素提供了一个平台.
科学领域:
- 有机化学
- 医学化学
- 微生物学
背景情况:
- 复杂发酵产品的半合成对于抗生素的发现至关重要.
- 细菌耐药性已经降低了现有的类抗生素的疗效.
研究的目的:
- 开发一种实用的全合成抗生素.
- 通过传统方法无法合成多种类结构.
主要方法:
- 简单的化学构件的融合组合.
- 合成了300多种新的宏类抗生素候选药物和临床候选药物索利特罗米.
主要成果:
- 开发的融合方法允许合成多样化的宏体结构.
- 大多数合成的化合物表现出抗生素活性.
- 一些化合物对抗抗现有宏素的细菌菌株有效.
结论:
- 描述的化学成分为发现新型宏类抗生素提供了多功能平台.
- 这种合成策略也可能适用于新抗生素的制造.
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