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新型强效抗菌恶唑烷酮类药物(MRX-I),具有改善的类安全性特征。

New potent antibacterial oxazolidinone (MRX-I) with an improved class safety profile.

机构信息

MicuRx Pharmaceuticals Inc. , Hayward, California 94545, United States.

出版信息

J Med Chem. 2014 Jun 12;57(11):4487-97. doi: 10.1021/jm401931e. Epub 2014 Apr 16.

DOI:10.1021/jm401931e
PMID:24694071
Abstract

Oxazolidinones comprise an important class of antibacterial protein synthesis inhibitors. Myelosuppression and monoamine oxidase inhibition (MAOI) are key independent causes for limiting adverse effects in therapy with the sole approved drug of this class, linezolid. This annotation describes a novel oxazolidinone agent, (S)-5-((isoxazol-3-ylamino)methyl)-3-(2,3,5-trifluoro-4-(4-oxo-3,4-dihydropyridin-1(2H)-yl)phenyl)oxazolidin-2-one (MRX-I), distinguished by its high activity against Gram-positive pathogens coupled with markedly reduced potential for myelosuppression and MAOI. The medical need, medicinal chemistry rationale, preclinical data, and phase I clinical trial summary for this new agent are reviewed herein.

摘要

恶唑烷酮类是一类重要的抗菌蛋白合成抑制剂。骨髓抑制和单胺氧化酶抑制(MAOI)是限制该类唯一批准药物利奈唑胺治疗中不良反应的关键独立因素。本注释描述了一种新型恶唑烷酮类药物(S)-5-((异噁唑-3-基氨基)甲基)-3-(2,3,5-三氟-4-(4-氧代-3,4-二氢吡啶-1(2H)-基)苯基)恶唑烷-2-酮(MRX-I),其特点是对革兰氏阳性病原体具有高活性,同时骨髓抑制和 MAOI 的潜力明显降低。本文综述了该新型药物的医疗需求、药物化学原理、临床前数据和 I 期临床试验总结。

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New potent antibacterial oxazolidinone (MRX-I) with an improved class safety profile.新型强效抗菌恶唑烷酮类药物(MRX-I),具有改善的类安全性特征。
J Med Chem. 2014 Jun 12;57(11):4487-97. doi: 10.1021/jm401931e. Epub 2014 Apr 16.
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