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AS-924,一种新型的头孢唑肟口服活性双功能前药。合成及其理化性质与口服吸收之间的关系。

AS-924, a novel orally active bifunctional prodrug of ceftizoxime. Synthesis and relationship between physicochemical properties and oral absorption.

作者信息

Kasai M, Hatano S, Kitagawa M, Yoshimi A, Nishimura K, Mori N, Sakai A, Sugihara T

机构信息

Research Laboratories, Kyoto Pharmaceutical Industries, Ltd., Japan.

出版信息

Chem Pharm Bull (Tokyo). 1999 Aug;47(8):1081-8. doi: 10.1248/cpb.47.1081.

Abstract

Ceftizoxime (CZX), a parenteral cephalosporin, has potent and broad antibacterial activity. To improve its oral absorption, we synthesized a series of monofunctional and bifunctional prodrugs of CZX. In rabbits, urinary recovery after oral administration of CZX was improved by esterification of the carboxyl group at the C-4 position with various lipophilic moieties (monofunctional prodrugs), and was further increased by introduction of a hydrophilic L-alanine to the amino group on the thiazole ring at the C-7 position (bifunctional prodrugs). Least-squares analysis showed good parabolic correlations between log P and urinary recovery for monofunctional and bifunctional prodrugs, respectively. AS-924, a bifunctional prodrug with a pivaloyloxymethyl and L-alanyl moiety had the best balance of lipophilicity and water-solubility for oral absorption among the prodrugs synthesized.

摘要

头孢唑肟(CZX)是一种肠胃外使用的头孢菌素,具有强大且广泛的抗菌活性。为提高其口服吸收效果,我们合成了一系列CZX的单功能和双功能前药。在兔子身上,通过用各种亲脂性基团酯化C-4位的羧基(单功能前药),口服CZX后的尿液回收率得到提高,并且通过在C-7位噻唑环上的氨基引入亲水性L-丙氨酸(双功能前药),回收率进一步提高。最小二乘法分析表明,单功能和双功能前药的log P与尿液回收率之间分别呈现良好的抛物线相关性。AS-924是一种具有新戊酰氧基甲基和L-丙氨酰部分的双功能前药,在所合成的前药中,其在口服吸收的亲脂性和水溶性方面具有最佳平衡。

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