Department of Applied Chemistry, College of Science , China Agricultural University , Beijing 100193 , China.
State Key Laboratory of Fine Chemicals and School of Life Science and Biotechnology , Dalian University of Technology , Dalian 116024 , China.
J Agric Food Chem. 2018 Apr 4;66(13):3351-3357. doi: 10.1021/acs.jafc.8b00017. Epub 2018 Mar 22.
Chitinases play a vital part in the molting phase of insect pests. Inhibiting their activities by the use of drug-like small chemical molecules is thought to be an efficient strategy in pesticide design and development. On the basis of the crystal structure of OfChtI, a chitinase indispensable for the molting of the insect pest Ostrinia furnacalis (Asian corn borer), here we report a chemical fragment and five variant compounds as inhibitors of OfChtI obtained from a library of over 200 000 chemicals by a structure-based-virtual-screening approach. The compounds were synthesized with high atom economy and tested for their OfChtI-inhibitory activities in a bioassay. Compound 3 showed preferential inhibitory activity with a K value of 1.5 μΜ against OfChtI. Analysis of the structure-activity relationships of the compounds provided insight into their interactions with the enzyme active site, which may inform future work in improving the potencies of their inhibitory activities.
几丁质酶在害虫的蜕皮阶段起着至关重要的作用。通过使用类似药物的小分子化合物来抑制它们的活性,被认为是农药设计和开发的一种有效策略。基于昆虫害虫亚洲玉米螟蜕皮所必需的几丁质酶 OfChtI 的晶体结构,我们在这里报告了一种从超过 20 万种化学物质的文库中通过基于结构的虚拟筛选方法获得的作为 OfChtI 抑制剂的化学片段和五个变体化合物。这些化合物以高原子经济性合成,并在生物测定中测试了它们对 OfChtI 的抑制活性。化合物 3 对 OfChtI 表现出优先的抑制活性,K 值为 1.5 μM。对化合物的构效关系分析提供了它们与酶活性位点相互作用的见解,这可能为提高它们抑制活性的效力提供信息。