Cui Chang-Yi, Liu Jun, Zheng Hong-Bo, Jin Xue-Yang, Zhao Xiao-Yu, Chang Wen-Qiang, Sun Bin, Lou Hong-Xiang
School of Pharmaceutical Sciences, Shandong University, Jinan 250012, PR China.
School of Pharmaceutical Sciences, Shandong University, Jinan 250012, PR China; National Glycoengineering Research Center, Shandong University, Jinan 250012, PR China.
Bioorg Med Chem Lett. 2018 May 15;28(9):1545-1549. doi: 10.1016/j.bmcl.2018.03.066. Epub 2018 Mar 24.
Diversity-oriented synthesis of derivatives of natural products is an important approach for the discovery of novel drugs. In this paper, a series of novel 3,4-diaryl-1H-pyrazoles and 3,5-diaryl-1H-pyrazoles derivatives were synthesized through the one-pot reaction of flavones and isoflavones with the hydrazine hydrate and substituted hydrazine hydrate. Some of these novel compounds exhibited antifungal effects against Candida albicans SC5314, and displayed more potent inhibitory activities against the efflux-pump-deficient strain DSY654. In addition, compounds 25, 28 and 32a displayed outstanding reversal activity of azole resistance against clinical azole-resistant Candida albicans in combination with fluconazole (FLC), with FICI values ranging from 0.012 to 0.141. The preliminary structure-activity relationship (SAR) of these compounds was also discussed. In conclusion, this study provides several novel agents that displayed potent antifungal activities alone or together with fluconazole, which makes progress for development of antifungal drugs.
天然产物衍生物的多样性导向合成是发现新型药物的重要途径。本文通过黄酮和异黄酮与水合肼及取代水合肼的一锅法反应,合成了一系列新型的3,4 - 二芳基 - 1H - 吡唑和3,5 - 二芳基 - 1H - 吡唑衍生物。其中一些新型化合物对白色念珠菌SC5314表现出抗真菌作用,并且对流出泵缺陷菌株DSY654显示出更强的抑制活性。此外,化合物25、28和32a与氟康唑(FLC)联合使用时,对临床唑类耐药的白色念珠菌表现出出色的唑类耐药逆转活性,FICI值范围为0.012至0.141。还讨论了这些化合物的初步构效关系(SAR)。总之,本研究提供了几种单独或与氟康唑一起显示出强效抗真菌活性的新型药物,这为抗真菌药物的开发取得了进展。