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原子水平的设计:作为高效口服活性抗生素的联芳基恶唑烷酮的设计

Design at the atomic level: design of biaryloxazolidinones as potent orally active antibiotics.

作者信息

Zhou Jiacheng, Bhattacharjee Ashoke, Chen Shili, Chen Yi, Duffy Erin, Farmer Jay, Goldberg Joel, Hanselmann Roger, Ippolito Joseph A, Lou Rongliang, Orbin Alia, Oyelere Ayomi, Salvino Joe, Springer Dane, Tran Jennifer, Wang Deping, Wu Yusheng, Johnson Graham

机构信息

Department of Medicinal Chemistry, Rib-X Pharmaceuticals Inc., 300 George Street, Suite 301, New Haven, CT 06511, USA.

出版信息

Bioorg Med Chem Lett. 2008 Dec 1;18(23):6175-8. doi: 10.1016/j.bmcl.2008.10.011. Epub 2008 Oct 7.

Abstract

We have developed a first generation of hybrid sparsomycin-linezolid compounds into a new family of orally bioavailable biaryloxazolidinones that have activity against both linezolid-susceptible and -resistant gram-positive bacteria as well as the fastidious gram-negative bacteria Haemophilus influenzae and Moraxella catarrahalis. The convergent synthesis of these new compounds is detailed.

摘要

我们已将第一代杂交的稀疏霉素-利奈唑胺化合物开发成一类新的口服生物可利用的联芳基恶唑烷酮,它们对利奈唑胺敏感和耐药的革兰氏阳性菌以及苛求革兰氏阴性菌流感嗜血杆菌和卡他莫拉菌均具有活性。详细介绍了这些新化合物的汇聚合成。

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