Suppr超能文献

N-芳基苯并喹哪啶鎓衍生物对一种临床菌株的抗真菌活性。

Antifungal Activity of N-Arylbenzoquinaldinium Derivatives against a Clinical Strain of .

作者信息

Shchepina Nadezhda E, Alexandrova Galina A, Balandina Svetlana Y, Boiko Igor I, Chaudhary Sandeep, Shchepin Roman V

机构信息

From the Laboratory of Radiochemistry, Natural Sciences Institute of Perm State University, Perm, Russia.

Laboratory 'Bactericide', Perm State University, Perm, Russia.

出版信息

Indian J Dermatol. 2023 Jul-Aug;68(4):487. doi: 10.4103/ijd.IJD_261_16.

Abstract

BACKGROUND

(Bodin, 1902) is a dermatophyte, which is widely represented in the developing and the developed world alike. Commonly transmitted from domestic animals it is particularly dangerous for immunosuppressed patients due to AIDS, cancer or transplant surgery. Search for new perspective antimycotic derivatives becomes an urgent task in the disease containment. Previously, several quinolinium analogs were screened for their antibacterial activity () by our research team. Furthermore, some phenylbenzoquinaldinium derivatives have shown antifungal activity against and .

AIMS

In this study, we sought to investigate fungicidal properties of arylbenzoquinaldinium derivatives against a clinical strain of for future medicinal applications.

MATERIALS AND METHODS

phenyl-[f]-benzoquinaldinium salts were prepared by a variation of the previously described technique and tested against a clinical strain of the fungus of harvested from pathogenic material of a patient (Perm, Russia, 2014).

RESULTS

phenyl-[f]-benzoquinaldinium tetrafluoroborate has shown antifungal activity par to (or exceeding) that of commercially available medication. Moreover, this benzoquinaldinium analog can be potentially labelled with tritium by our nuclear-chemical method, making it amenable for the sensitive pharmacokinetic studies.

CONCLUSIONS

-phenyl-[f]-benzoquinaldinium tetrafluoroborate has been shown as a promising compound for the further development of potent antifungal agents as well as radiotracers for further elucidation of biological pathways of antifungal activity.

摘要

背景

(博丹,1902年)是一种皮肤癣菌,在发展中国家和发达国家都广泛存在。它通常由家畜传播,对因艾滋病、癌症或移植手术而免疫抑制的患者尤其危险。寻找新的有前景的抗真菌衍生物成为控制该疾病的一项紧迫任务。此前,我们的研究团队筛选了几种喹啉鎓类似物的抗菌活性()。此外,一些苯基苯并喹啉鎓衍生物已显示出对和的抗真菌活性。

目的

在本研究中,我们试图研究芳基苯并喹啉鎓衍生物对一种临床菌株的杀菌特性,以供未来医学应用。

材料和方法

通过对先前描述技术的改进制备苯基-[f]-苯并喹啉鎓盐,并针对从一名患者(俄罗斯彼尔姆,2014年)的致病材料中分离出的该真菌的临床菌株进行测试。

结果

苯基-[f]-苯并喹啉鎓四氟硼酸盐已显示出与市售药物相当(或超过)的抗真菌活性。此外,这种苯并喹啉鎓类似物可以通过我们的核化学方法潜在地用氚标记,使其适用于灵敏的药代动力学研究。

结论

-苯基-[f]-苯并喹啉鎓四氟硼酸盐已被证明是一种有前景的化合物,可用于进一步开发强效抗真菌剂以及放射性示踪剂,以进一步阐明抗真菌活性的生物学途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/10564204/83ad668ce5c8/IJD-68-487c-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验