Suppr超能文献

黄烷酮衍生物的抗锥虫活性。

Trypanocidal Activity of Flavanone Derivatives.

机构信息

Chemistry Department, ICEB, Federal University of Ouro Preto, Campus Universitário Morro do Cruzeiro, Ouro Preto 35400-000, MG, Brazil.

René Rachou Institute, FIOCRUZ, Belo Horizonte 30190-002, MG, Brazil.

出版信息

Molecules. 2020 Jan 17;25(2):397. doi: 10.3390/molecules25020397.

Abstract

Chagas disease, also known as American trypanosomiasis, is classified as a neglected disease by the World Health Organization. For clinical treatment, only two drugs have been on the market, Benznidazole and Nifurtimox, both of which are recommended for use in the acute phase but present low cure rates in the chronic phase. Furthermore, strong side effects may result in discontinuation of this treatment. Faced with this situation, we report the synthesis and trypanocidal activity of 3-benzoyl-flavanones. Novel 3-benzoyl-flavanone derivatives were prepared in satisfactory yields in the 3-step synthetic procedure. According to recommended guidelines, the whole cell-based screening methodology was utilized that allowed for the simultaneous use of both parasite forms responsible for human infection. The majority of the tested compounds displayed promising anti- activity and the most potent flavanone bearing a nitrofuran moiety was more potent than the reference drug, Benznidazole.

摘要

恰加斯病,又称美洲锥虫病,被世界卫生组织列为被忽视的疾病。对于临床治疗,仅有两种药物上市,分别为苯唑硝唑和硝呋替莫,两者均被推荐用于急性期,但在慢性期的治愈率较低。此外,强烈的副作用可能导致治疗中断。面对这种情况,我们报告了 3-苯甲酰基黄酮的合成和杀锥虫活性。在三步合成过程中,以令人满意的产率制备了新型 3-苯甲酰基黄酮衍生物。根据推荐的指南,采用了基于全细胞的筛选方法,该方法允许同时使用引起人类感染的两种寄生虫形式。大多数测试化合物表现出有希望的抗活性,并且带有硝呋喃基团的最有效黄酮比参考药物苯唑硝唑更有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49f3/7024391/85b5f170256d/molecules-25-00397-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验