Mefentrifluconazole: The novel triazole fungicide

Nada Milutinović, M. Stević, Bojana Špirović-Trifunović, D. Brkić
{"title":"Mefentrifluconazole: The novel triazole fungicide","authors":"Nada Milutinović, M. Stević, Bojana Špirović-Trifunović, D. Brkić","doi":"10.5937/biljlek2304594m","DOIUrl":null,"url":null,"abstract":"Mefentrifluconazole is a new fungicidal active substance from the isopropanol-azoles, a new sub-class of triazoles. It inhibits sterols biosynthesis and is a very selective fungicide. It is a systemic fungicide with protective, curative, and eradicative activity. Its spectrum includes important pathogens of cereals (Septoria spp., Puccinia spp., Ramularia collocygni, Rhynchosporium secalis). Unlike most triazoles, withdrawn from use in the last 2-3 years, mainly due to reprotoxic and carcinogenic effects, mefentrifluconazole is neither carcinogenic, nor genotoxic or reprotoxic. In adition, it is not acutely toxic, is not irritant to skin or eyes and does not cause specific toxicity to target organs after single or repeated exposure. In contact with the skin, it can cause sensitization, and this is the only toxicological property on the basis of which it is classified and labeled. Acute and chronic dietary exposure of all population groups to this active substance is low, with a large margin of safety. Mefentrifluconazole is not acutely toxic to bees and earthworms. It is very toxic acutely and chronically for aquatic organisms, fish, invertebrates, and algae, while it is toxic for sediment organisms and aquatic macrophytes. The favourable toxicological properties of mefentrifluconazole, and good efficacy in control of important pathogens, recommend this active substance as a good substitute for withdrawn triazoles.","PeriodicalId":8829,"journal":{"name":"Biljni lekar","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biljni lekar","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5937/biljlek2304594m","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Mefentrifluconazole is a new fungicidal active substance from the isopropanol-azoles, a new sub-class of triazoles. It inhibits sterols biosynthesis and is a very selective fungicide. It is a systemic fungicide with protective, curative, and eradicative activity. Its spectrum includes important pathogens of cereals (Septoria spp., Puccinia spp., Ramularia collocygni, Rhynchosporium secalis). Unlike most triazoles, withdrawn from use in the last 2-3 years, mainly due to reprotoxic and carcinogenic effects, mefentrifluconazole is neither carcinogenic, nor genotoxic or reprotoxic. In adition, it is not acutely toxic, is not irritant to skin or eyes and does not cause specific toxicity to target organs after single or repeated exposure. In contact with the skin, it can cause sensitization, and this is the only toxicological property on the basis of which it is classified and labeled. Acute and chronic dietary exposure of all population groups to this active substance is low, with a large margin of safety. Mefentrifluconazole is not acutely toxic to bees and earthworms. It is very toxic acutely and chronically for aquatic organisms, fish, invertebrates, and algae, while it is toxic for sediment organisms and aquatic macrophytes. The favourable toxicological properties of mefentrifluconazole, and good efficacy in control of important pathogens, recommend this active substance as a good substitute for withdrawn triazoles.
甲苯三氟康唑:新型三唑类杀菌剂
甲苯三氟康唑是三唑类新亚类异丙醇唑衍生的一种新型杀真菌活性物质。它抑制甾醇的生物合成,是一种选择性很强的杀菌剂。它是一种具有保护、治疗和根除活性的全身性杀菌剂。它的谱包括谷物的重要病原体(Septoria spp., Puccinia spp., Ramularia collocygni, Rhynchosporium secalis)。与大多数三唑(主要由于生殖毒性和致癌作用而在过去2-3年停止使用)不同,甲氟康唑既不致癌,也没有遗传毒性或生殖毒性。此外,它没有急性毒性,对皮肤或眼睛没有刺激性,并且在一次或多次接触后不会对目标器官产生特异性毒性。在与皮肤接触时,它会引起致敏,这是它被分类和标记的唯一毒理学性质。所有人群对这种活性物质的急性和慢性饮食暴露量都很低,具有很大的安全边际。甲苯三氟康唑对蜜蜂和蚯蚓没有急性毒性。它对水生生物、鱼类、无脊椎动物和藻类有急性和慢性毒性,而对沉积物生物和水生植物有毒性。甲苯三氟康唑具有良好的毒理学特性,在控制重要病原体方面具有良好的疗效,因此推荐该活性物质作为已停用的三唑类药物的良好替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信