Structure-Based Virtual Screening, Compound Synthesis, and Bioassay for the Design of Chitinase Inhibitors.
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 200â¯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.
Palabras clave
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