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纳米氯化亚锡-二氧化硅,一种用于合成作为抗真菌和细胞毒性剂的苯并咪唑衍生物的高效催化剂。

Nano-SnCl.SiO, an efficient catalyst for synthesis of benzimidazole drivatives as antifungal and cytotoxic agents.

作者信息

Zamani Leila, Faghih Zeinab, Zomorodian Kamiar, Mirjalili Bi Bi Fatemeh, Jalilian Asghar, Khabnadideh Soghra

机构信息

Pharmaceutical Sciences Research Centre, Shiraz University of Medical Sciences, Shiraz, I.R. Iran.

Center of Basic Researches in Infectious Diseases, Department of Medical Mycology, and Parasitology School of Medicine, Shiraz University of Medical Sciences, Shiraz, I.R. Iran.

出版信息

Res Pharm Sci. 2019 Dec 11;14(6):496-503. doi: 10.4103/1735-5362.272536. eCollection 2019 Dec.

DOI:10.4103/1735-5362.272536
PMID:32038729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6937748/
Abstract

The concept of green chemistry has made significant impact on many frontages including the use of green solvents or sustainable catalyst materials. Benzimidazole ring is an important nitrogen-containing heterocyclic, which exhibits a broad spectrum of bioactivities and are widely utilized by the medicinal chemists for drug discovery. A simple and efficient method was developed for the synthesis of some benzimidazole derivatives reaction of -phenylenediamine and substituted aldehydes in the presence of nano-SnCl/SiO as a mild catalyst. Ten 2-substituted benzimidazole compounds ( ) were synthesized. All compounds were evaluated against different species of yeasts and filament fungi using broth micro dilution method as recommended by clinical and laboratory standard institute. Among these compounds, the active ones were chosen for their cytotoxic activities evaluation against MCF-7 and A549 cell lines using MTT method. Compound showed the best antifungal activity against all tested species. Compounds had also desirable antifungal activities. Our cytotoxic results were also similar to the antifungal activities except for which had no cytotoxic activity.

摘要

绿色化学的概念已在许多方面产生了重大影响,包括绿色溶剂的使用或可持续催化剂材料。苯并咪唑环是一种重要的含氮杂环,具有广泛的生物活性,被药物化学家广泛用于药物发现。开发了一种简单有效的方法,用于在纳米SnCl/SiO作为温和催化剂的存在下,通过对苯二胺与取代醛的反应合成一些苯并咪唑衍生物。合成了十种2-取代苯并咪唑化合物( )。按照临床和实验室标准研究所的建议,使用肉汤微量稀释法对所有化合物针对不同种类的酵母和丝状真菌进行了评估。在这些化合物中,选择活性化合物使用MTT法对MCF-7和A549细胞系进行细胞毒性活性评估。化合物 对所有测试物种表现出最佳的抗真菌活性。化合物 也具有理想的抗真菌活性。除了没有细胞毒性活性的 之外,我们的细胞毒性结果也与抗真菌活性相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5be6/6937748/aa3c3e65da63/RPS-14-496-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5be6/6937748/aa3c3e65da63/RPS-14-496-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5be6/6937748/aa3c3e65da63/RPS-14-496-g001.jpg

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