Novel metronidazole-chalcone conjugates with potential to counter drug resistance in Trichomonas vaginalis

被引:25
作者
Anthwal, Amit [1 ,2 ]
Rajesh, U. Chinna [2 ]
Rawat, M. S. M. [1 ]
Kushwaha, Bhavana [3 ]
Maikhuri, Jagdamba P. [3 ]
Sharma, Vishnu L. [4 ]
Gupta, Gopal [3 ]
Rawat, Diwan S. [2 ]
机构
[1] HNB Garhwal Univ, Dept Chem, Srinagar 246174, Uttarakhand, India
[2] Univ Delhi, Dept Chem, Delhi 110007, India
[3] CSIR, Cent Drug Res Inst, Div Endocrinol, Lucknow 226031, Uttar Pradesh, India
[4] CSIR, Cent Drug Res Inst, Div Med & Proc Chem, Lucknow 226031, Uttar Pradesh, India
关键词
Trichomonas vaginalis; Metronidazole; Drug resistance; HeLa cell line; BIOLOGICAL EVALUATION; ANTIOXIDANT; ANTICANCER; DERIVATIVES; DESIGN;
D O I
10.1016/j.ejmech.2014.03.076
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Trichomoniasis is the most prevalent, curable sexually transmitted disease (STD), which increases risk of viral STDs and HIV. However, drug resistance has been developed by some strains of Trichomonas vaginalis against Metronidazole (MTZ), the FDA approved drug against trichomoniasis. In the present study twenty two chalcone hybrids of metronidazole have been synthesized in a quest to get new molecules with higher potential against metronidazole-resistant T vaginalis. All new hybrid molecules were found active against T vaginalis with varying levels of activity against MTZ-susceptible and resistant strains. Eight compounds (4a, 4c, 4d, 4e, 4f, 4h, 4q and 4s) were found as active as the standard drug with an MIC of 1.56 mu g/m1 against MTZ-susceptible strain. However, compounds 4e, 4h and 4m were 4-times more active than MTZ against drug-resistant T vaginalis, amongst which 4e and 4h were most promising against both susceptible and resistant strains. (C) 2014 Published by Elsevier Masson SAS.
引用
收藏
页码:89 / 94
页数:6
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