Design, synthesis and SAR studies of N'-(Ethynylsalicylidene)arenecarbohydrazides as next-generation broad-spectrum antifungal agents

N'-(乙炔基水杨醛)芳烃碳酰肼类化合物作为下一代广谱抗真菌剂的设计、合成及构效关系研究

阅读:6

Abstract

The present study investigated whether bromine could be replaced with its bioisostere, ethynyl group, without losing potency and selectivity toward fungi, and has found that the bioisosteric replacement strategy is successfully applied to the design, synthesis and SAR study of novel 2nd-generation N'-(salicylidene)arenecarbohydrazides, bearing ethynyl groups. This study particularly focused on the broad-spectrum antifungal activities against three critical priority fungal pathogens, C. neoformans, C. albicans, and A. fumigatus to select highly promising lead compounds. Reliable QSAR models for optimization and further drug development have been successfully created using the AutoQSAR program. Also, in silico ADME/Tox predictions were performed, which predicted considerably improved ClogP values (3.26-5.66), no mutagenicity (AMES test) except for 2 compounds (with low confidence) out of 31, no hERG toxicity, no lethal toxicity (LD(50) > 2 Mol/kg), no hepatotoxicity except for 2 compounds out of 31, and good Caco2 permeability. This study has identified 3 compounds, 8.1, 8.6 and 8.23 as the most promising leads for further drug development, which exhibited excellent broad-spectrum antifungal activities against the three fungal pathogens with high (SI >100) to extremely high (SI up to 17,066) selectivity indices and relevant ClogP values (3.26-4.40). Compounds 8.1 and 8.23 showed synergy in combination with 3 clinical antifungal drugs, especially 8.1 exhibited synergy with 3 clinical drugs against all 3 distinctly different fungal pathogens. Compound 8.23 will serve as the scaffold for developing a new series of bromine-free N'-(salicylidene)arene(or heteroarene)carbohydrazides.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。