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吡唑并[3,4 - d][1,2,3]三唑 - 1 - 甲酰胺和5 - 烷基氨基吡唑并[3,4 - d]恶唑:体外抗真菌活性的合成与评价

Pyrazolo[3,4-d][1,2,3]triazole-1-carboxamides and 5-alkylaminopyrazolo[3,4-d]oxazoles: synthesis and evaluation of the in vitro antifungal activity.

作者信息

Vicentini C B, Brandolini V, Guarneri M, Giori P

机构信息

Dipartimento di Scienze Farmaceutiche Università di Ferrara, Italy.

出版信息

Farmaco. 1992 Jul-Aug;47(7-8):1021-34.

PMID:1445610
Abstract

A series of N-alkyl-N'-(4-diazo-5-pyrazolyl)-ureas (4) was thermally and photochemically converted into pyrazolo [3,4-d][1,2,3]triazole derivatives (5,6) and 5-alkylaminopyrazolo[3,4-d]oxazoles (7) respectively. The products were tested for in vitro antifungal activity against Fusarium culmorum, Botrytis cinerea, Phoma betae, Pythium ultimum, Sclerotinia minor and Rhizoctonia solani. The MIC and ED50 values of compound (6) against some of the test fungi were comparable to those of the reference fungicides iprodione and mancozeb.

摘要

一系列N-烷基-N'-(4-重氮-5-吡唑基)脲(4)分别经热化学和光化学转化为吡唑并[3,4-d][1,2,3]三唑衍生物(5,6)和5-烷基氨基吡唑并[3,4-d]恶唑(7)。测试了这些产物对禾谷镰刀菌、灰葡萄孢、甜菜茎点霉、终极腐霉、核盘菌和立枯丝核菌的体外抗真菌活性。化合物(6)对某些测试真菌的MIC和ED50值与参比杀菌剂异菌脲和代森锰锌相当。

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