SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SOME DERIVATIVES OF RIFAMYCIN-P

被引:18
作者
CAVALLERI, B
TURCONI, M
TAMBORINI, G
OCCELLI, E
CIETTO, G
PALLANZA, R
SCOTTI, R
BERTI, M
ROMANO, G
PARENTI, F
机构
[1] Istituto De Angeli S.p.A., Milano
[2] Merrell Dow Research Institute-Lepetit Research Center, via R. Lepetit 34, 21040, Gerenzano (Va)
关键词
D O I
10.1021/jm00167a029
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of derivatives of rifamycin P, an antibiotic produced by fermentation of a mutant strain of Nocardia mediterranea or by chemical modification of rifamycin S, have been prepared. The structures of these compounds were determined by 1H NMR, IR, UV, and LC/MS. Their in vitro and in vivo antibacterial activities in comparison with rifampicin and two other rifamycins under investigation were evaluated. The derivatives were more active than rifamycin P against Mycobacterium avium complex and other slowly and rapidly growing nontuberculous mycobacteria which frequently cause systemic infection in patients with AIDS. 2'-(Diethylamino)rifamycin P (P/DEA) appears suitable for further investigation. © 1990, American Chemical Society. All rights reserved.
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页码:1470 / 1476
页数:7
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