天然产物
金黄色葡萄球菌
班级(哲学)
计算机科学
多样性(政治)
膦酸盐
药物发现
耐甲氧西林金黄色葡萄球菌
产品(数学)
万维网
计算生物学
化学
生物
立体化学
生物信息学
细菌
社会学
数学
人工智能
生物化学
遗传学
几何学
人类学
作者
Gemma L. Thomas,Richard J. Spandl,Freija G. Glansdorp,Martin Welch,Andreas Bender,Joshua Cockfield,Jodi A. Lindsay,Clare Bryant,Derek F. J. Brown,Olivier Loiseleur,Hélène Rudyk,Mark Ladlow,David R. Spring
标识
DOI:10.1002/anie.200705415
摘要
Beating the superbugs: Diversity-oriented synthesis using a solid-supported phosphonate unit to synthesize 242 drug-like compounds based on 18 natural-product-like scaffolds led to the discovery of gemmacin (see scheme). This new structural class of antibiotic is active towards methicillin-resistant Staphylococcus aureus (MRSA). Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2008/z705415_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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