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新型哌啶氧基恶唑烷酮类抗菌剂。N-取代基的多样化。

Novel piperidinyloxy oxazolidinone antibacterial agents. Diversification of the N-Substituent.

作者信息

Weidner-Wells Michele A, Boggs Christine M, Foleno Barbara D, Melton John, Bush Karen, Goldschmidt Raul M, Hlasta Dennis J

机构信息

Antimicrobial Agents Research Team, Johnson and Johnson Pharmaceutical Research and Development, LLC, 1000 Route 202, Raritan, NJ 08869, USA.

出版信息

Bioorg Med Chem. 2002 Jul;10(7):2345-51. doi: 10.1016/s0968-0896(02)00065-2.

Abstract

Oxazolidinone antibacterial agents, where the morpholino group of linezolid was replaced with an N-substituted piperidinyloxy moiety, were synthesized and shown to be active against a variety of resistant and susceptible Gram-positive organisms. The functionality attached to the piperidine nitrogen was varied extensively to determine the SAR for this series. One of the most potent compounds, 11, showed in vivo efficacy upon subcutaneous administration in a Staphylococcus aureus Smith murine systemic infection.

摘要

恶唑烷酮类抗菌剂中,利奈唑胺的吗啉基团被N-取代的哌啶氧基部分所取代,已合成并显示对多种耐药和敏感的革兰氏阳性菌具有活性。广泛改变连接在哌啶氮上的官能团以确定该系列的构效关系。其中一种最有效的化合物11,在金黄色葡萄球菌史密斯小鼠全身感染模型中皮下给药后显示出体内疗效。

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