Synthesis and in vitro selective anti-Helicobacter pylori activity of N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides

被引:52
作者
Chimenti, F
Bizzarri, B
Bolasco, A
Secci, D
Chimenti, P
Carradori, S
Granese, A
Rivanera, D
Lilli, D
Scaltrito, MM
Brenciaglia, MI
机构
[1] Univ Roma La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biol At, I-00185 Rome, Italy
[2] Univ Roma La Sapienza, Dipartimento Sci Sanita Pubbl, I-00185 Rome, Italy
[3] Univ Milan, Ist Microbiol, I-20133 Milan, Italy
关键词
Coumarin; antibacterial activity; anti-Helicobacter pylori activity;
D O I
10.1016/j.ejmech.2005.11.001
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
In order to develop new anti-Helicobacter pylori agents, five new and three already known N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides (coumarin-3-carboxamides) were prepared and evaluated for their antibacterial activity. All synthesized compounds showed little or no activity against different species of Gram-positive and Gram-negative bacteria of clinical relevance and against various strains of pathogenic fungi. Among the prepared compounds those with a 4-acyl-phenyl group showed the best activity against H. pylori metronidazole resistant strains in the 0.25-1 mu g/ml MIC range, indicating the presence of an acyl function as an important feature for activity. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:208 / 212
页数:5
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