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设计、合成及吡唑噻唑甲酰胺衍生物的杀菌活性。

Design, synthesis and fungicidal activity of pyrazole-thiazole carboxamide derivatives.

机构信息

State Key Laboratory of Elemento-Organic Chemistry, College of Chemistry, Nankai University, No. 94, Weijin Road, Nankai District, Tianjin, 300071, People's Republic of China.

出版信息

Mol Divers. 2022 Feb;26(1):205-214. doi: 10.1007/s11030-020-10177-0. Epub 2021 Apr 1.

Abstract

Twenty-one novel pyrazole-thiazole carboxamide derivatives were rationally designed and synthesized. Bioassay results indicated that 6d (EC = 5.11 μg/mL) and 6j (EC = 8.14 μg/mL) exhibited better in vitro activities than fluxapyroxad (EC = 11.93 μg/mL) and thifluzamide (EC = 22.12 μg/mL) against Rhizoctonia cerealis. Particularly, compound 6j showed promising in vivo protective activity against Rhizoctonia solani and Puccinia sorghi Schw. with 80% and 90% inhibition at 10 μg/mL, respectively. Our studies found that pyrazole-thiazole is a promising fungicide lead deserving for further derivation.

摘要

二十一种新型吡唑噻唑甲酰胺衍生物被合理设计和合成。生物测定结果表明,化合物 6d(EC=5.11μg/mL)和 6j(EC=8.14μg/mL)对禾谷丝核菌的体外活性优于氟环唑(EC=11.93μg/mL)和噻呋酰胺(EC=22.12μg/mL)。特别是,化合物 6j 对丝核菌和高粱坚黑粉菌表现出有希望的体内保护活性,在 10μg/mL 时分别抑制率达到 80%和 90%。我们的研究发现,吡唑噻唑是一种很有前途的杀菌剂先导化合物,值得进一步衍生。

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