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3-甲氧基甲基头孢菌素前药的合成及药代动力学特征

Synthesis and pharmacokinetic profile of 3-methoxymethyl cephalosporin prodrugs.

作者信息

Jung M H, Cho K W, Park J G, Kim Y H

机构信息

Korea Research Institute of Chemical Technology, Yusong, Taejon, Korea.

出版信息

Arch Pharm Res. 1998 Oct;21(5):559-64. doi: 10.1007/BF02975375.

Abstract

Preparation and biological activity of prodrug-type 3-methoxymethyl cephalosporins were described. From the mixtures, R- and S-prodrugs were separated and their absolute configurations were determined, and also their bioavailability was investigated.

摘要

描述了前药型3-甲氧基甲基头孢菌素的制备及其生物活性。从混合物中分离出R-和S-前药,测定了它们的绝对构型,并研究了它们的生物利用度。

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