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红霉素衍生物抗菌活性构效关系研究进展
引用本文:尹戎,包凯,张为革,程卯生. 红霉素衍生物抗菌活性构效关系研究进展[J]. 中国药物化学杂志, 2008, 18(3): 222-227
作者姓名:尹戎  包凯  张为革  程卯生
作者单位:沈阳药科大学,制药工程学院,辽宁,沈阳110016
摘    要:为解决抗生素的耐药性问题,近年来在红霉素化学结构修饰方面开展了大量的研究,并发现了诸如酮内酯、酰内酯、双环内酯等多种具有良好抗耐药菌活性的新型大环内酯类化合物。该文对红霉素衍生物抗菌活性研究成果做一概括,并对构效关系研究的某些重要结论加以探讨。

关 键 词:红霉素衍生物  抗菌活性  构效关系
文章编号:1005-0108(2008)03-0222-06
收稿时间:2007-11-05
修稿时间:2007-11-05

Recent development in the structure-activity relationships for the antimicrobial activity of erythromycin derivatives
YIN Rong,BAO Kai,ZHANG Wei-ge,CHENG Mao-sheng. Recent development in the structure-activity relationships for the antimicrobial activity of erythromycin derivatives[J]. Chinese Journal of Medicinal Chemistry, 2008, 18(3): 222-227
Authors:YIN Rong  BAO Kai  ZHANG Wei-ge  CHENG Mao-sheng
Affiliation:School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, China
Abstract:To address the problem of antibiotic resistance, tremendous efforts had been devoted to the chemical modification of erythromycin during the past several years. As a consequence, several novel series of macrolides, such as ketolide, acylide, bicyclolide, etc., had been recognized to be highly effective against macrolide-resistant pathogens. In this review, the recent progress on the antimicrobial research area of erythromycin derivatives were summarized and some important conclusions regarding structure-activity relationships were also discussed.
Keywords:erythromycin derivatives  antimicrobial activity  structure-activity relationship
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