用户名: 密码: 验证码:
1,2,3-Triazole pharmacophore-based benzofused nitrogen/sulfur heterocycles with potential anti-Moraxella catarrhalis activity
详细信息    查看全文
文摘
Versatile 1,2,3-triazole pharmacophore-based benzofused heterocycles containing halogen-substituted aromatic (917 and 2528), 7-substituted coumarin (1823 and 2930) or penciclovir-like subunit (31a,b38a) were designed and synthesized to evaluate their antibacterial activities against selected Gram-positive and Gram-negative bacteria. Hybridization approach using environmentally friendly Cu(I)-catalyzed click reaction under microwave irradiation was adopted in the synthesis of regioselective 1,4-disubstituted 1,2,3-triazole tethered heterocycles (923 and 2530), while post-N-alkylation of NH-1,2,3-triazoles afforded both 2,4- (31a38a) and 1,4-disubstituted (31b33b, 35b37b) 1,2,3-triazole regioisomers. The compounds 1823 and 2530 revealed fluorescence in the violet region of the visible spectrum with a strong influence of phenyl spacer in 2530 on both wavelength and emission intensity. Fusion of selected subunits led to new hybrid architecture, benzothiazole–1,2,3-triazole–coumarin 29 that demonstrated extremely narrow spectrum activity towards fastidious Gram-negative bacteria Moraxella catarrhalis. Selected hybrid showed the potency against Moraxella catarrhalis (MIC ⩽ 0.25 μg/mL) comparable to that of reference antibiotic azithromycin, which suggested that further investigations are necessary to optimize this potential hit compound as a new anti-Moraxella catarrhalis agent.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700