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发现具有强效广谱抗真菌活性的含苄氧基苯异噁唑侧链的新型三唑类化合物。

Discovery of novel triazoles containing benzyloxy phenyl isoxazole side chain with potent and broad-spectrum antifungal activity.

机构信息

Department of Pharmacy, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, No. 1239 Siping Road, Shanghai 200092, China; School of Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, 110016, China.

School of Pharmacy, Naval Medical University, No. 325 Guohe Road, Shanghai 200433, China.

出版信息

Bioorg Chem. 2023 Aug;137:106572. doi: 10.1016/j.bioorg.2023.106572. Epub 2023 Apr 28.

Abstract

As a continuation study, 29 novel triazoles containing benzyloxy phenyl isoxazole side chain were designed and synthesized based on our previous work. The majority of the compounds exhibited high potency in vitro antifungal activities against eight pathogenic fungi. The most active compounds 13, 20 and 27 displayed outstanding antifungal activity with MIC values ranging from <0.008 µg/mL to 1 µg/mL, and showed potent activity against six drug-resistant Candida auris isolates. Growth curve assays further confirmed the high potency of these compounds. Moreover, compounds 13, 20 and 27 showed a potent inhibitory activity on biofilm formation of C. albicans SC5314 and C. neoformans H99. Notably, compound 13 showed no inhibition of human CYP1A2 and low inhibitory activity against CYP2D6 and CYP3A4, suggesting a low risk of drug-drug interactions. With high potency in vitro and in vivo and good safety profiles, compound 13 will be further investigated as a promising candidate.

摘要

作为延续性研究,在我们以前的工作基础上,设计并合成了 29 种新型含苄氧基苯异噁唑侧链的三唑类化合物。大多数化合物表现出对八种致病性真菌的高体外抗真菌活性。最具活性的化合物 13、20 和 27 表现出优异的抗真菌活性,MIC 值范围为 <0.008µg/mL 至 1µg/mL,并且对六种耐氟康唑的耳念珠菌分离株表现出强大的活性。生长曲线测定进一步证实了这些化合物的高效性。此外,化合物 13、20 和 27 对白色念珠菌 SC5314 和新生隐球菌 H99 的生物膜形成具有很强的抑制作用。值得注意的是,化合物 13 对人 CYP1A2 没有抑制作用,对 CYP2D6 和 CYP3A4 的抑制活性较低,提示药物相互作用的风险较低。化合物 13 具有高体外和体内活性和良好的安全性特征,将作为一种有前途的候选药物进一步研究。

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