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新型吡唑呋喃和吡唑吡咯甲酰胺作为琥珀酸脱氢酶抑制剂的设计、合成与杀菌活性评价。

Design, Synthesis, and Fungicidal Evaluation of Novel Pyrazole-furan and Pyrazole-pyrrole Carboxamide as Succinate Dehydrogenase Inhibitors.

机构信息

Institute of Pesticide and Environmental Toxicology, Ministry of Agriculture Key Lab of Molecular Biology of Crop Pathogens and Insects, Zhejiang University , Hangzhou 310029, P. R. China.

ZJU-ENS Joint Laboratory of Medicinal Chemistry, Zhejiang Province Key Laboratory of Anti-Cancer Drug Research, College of Pharmaceutical Sciences, Zhejiang University , Hangzhou, 310058, P. R. China.

出版信息

J Agric Food Chem. 2017 Jul 5;65(26):5397-5403. doi: 10.1021/acs.jafc.7b01251. Epub 2017 Jun 26.

Abstract

The identification of novel succinate dehydrogenase (SDH) inhibitors represents one of the most attractive directions in the field of fungicide research and development. During our continuous efforts to pursue inhibitors belonging to this class, some structurally novel pyrazole-furan carboxamide and pyrazole-pyrrole carboxamide derivatives have been discovered via the introduction of scaffold hopping and bioisosterism to compound 1, a remarkably potent lead obtained by pharmacophore-based virtual screening. As a result of the evaluation against three destructive fungi, including Sclerotinia sclerotiorum, Rhizoctonia solani, and Pyricularia grisea, a majority of them displayed potent fungicidal activities. In particular, compounds 12I-i, 12III-f, and 12III-o exhibited excellent fungicidal activity against S. sclerotiorum and R. solani comparable to that of commercial SDHI thifluzamide and 1.

摘要

新型琥珀酸脱氢酶(SDH)抑制剂的鉴定是杀菌剂研发领域最具吸引力的方向之一。在我们不断努力寻找属于此类抑制剂的过程中,通过引入支架跃迁和生物等排原理,对基于药效团的虚拟筛选得到的显著有效先导化合物 1 进行了结构新颖的吡唑呋喃甲酰胺和吡唑吡咯甲酰胺衍生物的探索,得到了一些此类化合物。对包括核盘菌、立枯丝核菌和稻瘟病菌在内的三种破坏性真菌的评估结果表明,大多数化合物具有很强的杀菌活性。特别是化合物 12I-i、12III-f 和 12III-o 对核盘菌和立枯丝核菌的杀菌活性与商业 SDHI 噻呋酰胺和 1 相当。

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