Аннотация:
Free energy perturbation (FEP)-based molecular modeling simulation of 5-fluoropyrimidine and 1,3,5-triazine derivatives followed by their synthesis and experimental evaluation have been carried out to estimate kinase selectivity profile. 5-Fluoropyrimidine derivatives show similar binding affinity for c-Src, Btk and Jak1 kinases, while 1,3,5-triazine derivatives demonstrate c-Src kinase selectivity.
Реферативные базы данных:
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
V. S. Stroylov, D. V. Katkov, I. Yu. Titov, O. V. Stroganov, F. N. Novikov, G. G. Chilov, I. Svitanko, “Modeling comparative selectivity profiles of kinase inhibitors using FEP/MD protocol”, Mendeleev Commun., 27:4 (2017), 349–351