FMS-like tyrosine kinase 3(FLT3)is validated as a therapeutic target for AML treatment1.We firstly reported pteridin-7(8H)-one scaffold as potent FLT3 inhibitors derived from structural optimizations
Prediction of sites of metabolism(SOMs)mediated by cytochromes P450(CYPs)is of high interest in the drug discovery and development.In this work,we systematically evaluated the effects of receptor flex
Peptides play a crucial in controlling and modulating protein-protein interactions and gain a wide research interest.However,rational design of therapeutic peptides with high affinity has been a major
Computational prediction of drug-target interactions(DTIs)and drug repositioning provide low cost and high efficient ways for drug discovery.Recently,network-based approaches derived from recommendati