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Structure-Based Virtual Screening, Compound Synthesis, and Bioassay for the Design of Chitinase Inhibitors.
Dong, Yawen; Jiang, Xi; Liu, Tian; Ling, Yun; Yang, Qing; Zhang, Li; He, Xiongkui.
Afiliación
  • Dong Y; Department of Applied Chemistry, College of Science , China Agricultural University , Beijing 100193 , China.
  • Jiang X; State Key Laboratory of Fine Chemicals and School of Life Science and Biotechnology , Dalian University of Technology , Dalian 116024 , China.
  • Liu T; State Key Laboratory of Fine Chemicals and School of Life Science and Biotechnology , Dalian University of Technology , Dalian 116024 , China.
  • Ling Y; Department of Applied Chemistry, College of Science , China Agricultural University , Beijing 100193 , China.
  • Yang Q; State Key Laboratory of Fine Chemicals and School of Life Science and Biotechnology , Dalian University of Technology , Dalian 116024 , China.
  • Zhang L; Department of Applied Chemistry, College of Science , China Agricultural University , Beijing 100193 , China.
  • He X; Department of Applied Chemistry, College of Science , China Agricultural University , Beijing 100193 , China.
J Agric Food Chem ; 66(13): 3351-3357, 2018 Apr 04.
Article en En | MEDLINE | ID: mdl-29554796
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 Ki 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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quitinasas / Proteínas de Insectos / Inhibidores Enzimáticos / Mariposas Nocturnas Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: J Agric Food Chem Año: 2018 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Quitinasas / Proteínas de Insectos / Inhibidores Enzimáticos / Mariposas Nocturnas Tipo de estudio: Diagnostic_studies / Screening_studies Idioma: En Revista: J Agric Food Chem Año: 2018 Tipo del documento: Article País de afiliación: China