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新型苯并噻唑衍生物作为D1蛋白酶潜在抑制剂的合成与除草活性评价

Synthesis and herbicidal evaluation of novel benzothiazole derivatives as potential inhibitors of D1 protease.

作者信息

Huang Tonghui, Sun Jie, An Lin, Zhang Lixian, Han Cuiping

机构信息

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, School of Pharmacy, Xuzhou Medical College, Xuzhou, Jiangsu 221004, PR China; Key Laboratory of Pesticide and Chemical Biology of Ministry of Education, Central China Normal University, Wuhan 430079, PR China.

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, School of Pharmacy, Xuzhou Medical College, Xuzhou, Jiangsu 221004, PR China.

出版信息

Bioorg Med Chem Lett. 2016 Apr 1;26(7):1854-9. doi: 10.1016/j.bmcl.2016.01.087. Epub 2016 Feb 13.

Abstract

D1 protease is a C-terminal processing protease that has been predicted to be an ideal herbicidal target. Three novel series of benzothiazole derivatives were synthesized and evaluated for their herbicidal activities against Brassica napus (rape) and Echinochloa crusgalli (barnyard grass). The preliminary bioassay indicated that most of the synthesized compounds possess promising D1 protease inhibitory activities and considerable herbicidal activities. Molecular docking was performed to position representative compounds into the active site of D1 protease to determine a probable binding model.

摘要

D1蛋白酶是一种C末端加工蛋白酶,已被预测为理想的除草靶点。合成了三个新型苯并噻唑衍生物系列,并评估了它们对甘蓝型油菜(油菜)和稗草的除草活性。初步生物测定表明,大多数合成化合物具有良好的D1蛋白酶抑制活性和显著的除草活性。进行了分子对接,将代表性化合物定位到D1蛋白酶的活性位点,以确定可能的结合模式。

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