Glucosinolate derivatives as antifungals: A review.

IF 6.1 2区 医学 Q1 CHEMISTRY, MEDICINAL Phytotherapy Research Pub Date : 2024-11-01 Epub Date: 2024-08-05 DOI:10.1002/ptr.8307
Shivani Patil, Tanjila Gavandi, Sankunny Mohan Karuppayil, Ashwini Jadhav
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Abstract

Fungal infections are becoming a severe threat to the security of global public health due to the extensive use of antibiotic medications and the rise in immune-deficient patients globally. Additionally, there is an increase in the development of fungus resistance to available antifungal medications. It is necessary to focus on the development of new antifungal medications in order to address these problems. The wide range of chemical structures, low cost, high availability, high antimicrobial action, and lack of adverse effects are the characteristics of plant secondary metabolites. In order to find and develop new antifungal medications, plant secondary metabolites like glucosinolate (GSL) derivatives are crucial sources of information. These natural compounds are enzymatically transformed into isothiocyanates (ITCs), nitriles, epithionitriles, oxazolidin-2-thion, and thiocyanate when they get mechanically damaged. The current review offers a thorough understanding of how isothiocyanates affect fungi with detailed mechanism. Along with this antifungal activity of nitriles, epithionitriles, oxazolidin-2-thion, and thiocyanate are mentioned. The review summarizes our present understanding of the following subjects: role of isothiocyanate by inhibiting aflatoxin biosynthesis, effect of isothiocyanate on transcriptomes, isothiocyanate targets cell membrane, role of isothiocyanate in efflux, and the role of isothiocyanate in synergistic activity. Antifungal activity of nitrile, epithionitrile, oxazolidine-2-thion, and thiocyanate is mentioned. Cytotoxicity study and clinical trials data were also added. More extensive studies will be needed in this field to assess safety concerns and clinical efficacies of GSL derivatives.

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作为抗真菌药的葡萄糖苷酸衍生物:综述。
由于抗生素药物的广泛使用和全球免疫缺陷患者的增加,真菌感染正成为全球公共卫生安全的严重威胁。此外,真菌对现有抗真菌药物的耐药性也在增加。为了解决这些问题,有必要重点开发新型抗真菌药物。植物次生代谢物具有化学结构广泛、成本低、可获得性高、抗菌作用强、无不良反应等特点。为了寻找和开发新的抗真菌药物,葡萄糖苷酸(GSL)衍生物等植物次生代谢物是重要的信息来源。这些天然化合物在受到机械损伤时,会通过酶促作用转化为异硫氰酸盐(ITC)、腈类、表硫腈类、噁唑烷-2-硫酮和硫氰酸盐。本综述全面介绍了异硫氰酸盐如何影响真菌以及详细的机理。此外,还提到了腈类、表硫腈类、噁唑烷-2-硫酮和硫氰酸盐的抗真菌活性。综述总结了我们目前对以下主题的理解:异硫氰酸盐抑制黄曲霉毒素生物合成的作用、异硫氰酸盐对转录组的影响、异硫氰酸盐靶向细胞膜、异硫氰酸盐在外流中的作用以及异硫氰酸盐在协同作用中的作用。提到了腈、表噻腈、噁唑烷-2-硫酮和硫氰酸盐的抗真菌活性。还补充了细胞毒性研究和临床试验数据。该领域需要进行更广泛的研究,以评估 GSL 衍生物的安全性问题和临床疗效。
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来源期刊
Phytotherapy Research
Phytotherapy Research 医学-药学
CiteScore
12.80
自引率
5.60%
发文量
325
审稿时长
2.6 months
期刊介绍: Phytotherapy Research is an internationally recognized pharmacological journal that serves as a trailblazing resource for biochemists, pharmacologists, and toxicologists. We strive to disseminate groundbreaking research on medicinal plants, pushing the boundaries of knowledge and understanding in this field. Our primary focus areas encompass pharmacology, toxicology, and the clinical applications of herbs and natural products in medicine. We actively encourage submissions on the effects of commonly consumed food ingredients and standardized plant extracts. We welcome a range of contributions including original research papers, review articles, and letters. By providing a platform for the latest developments and discoveries in phytotherapy, we aim to support the advancement of scientific knowledge and contribute to the improvement of modern medicine.
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