Investigating the Selectivity of Allosteric Inhibitors for Mutant T790M EGFR over Wild Type Using Molecular Dynamics and Binding Free Energy Calculations
Main Authors: | Annachiara Tinivella, Giulio Rastelli |
---|---|
Format: | Article |
Language: | English |
Published: |
American Chemical Society
2018-12-01
|
Series: | ACS Omega |
Online Access: | http://dx.doi.org/10.1021/acsomega.8b03256 |
Similar Items
-
Prediction of activity and selectivity profiles of human Carbonic Anhydrase inhibitors using machine learning classification models
by: Annachiara Tinivella, et al.
Published: (2021-03-01) -
Mutational monitoring of EGFR T790M in cfDNA for clinical outcome prediction in EGFR-mutant lung adenocarcinoma.
by: Kang-Yi Su, et al.
Published: (2018-01-01) -
Autophagosome-mediated EGFR down-regulation induced by the CK2 inhibitor enhances the efficacy of EGFR-TKI on EGFR-mutant lung cancer cells with resistance by T790M.
by: Kwang Sup So, et al.
Published: (2014-01-01) -
A case report of EGFR mutant lung adenocarcinoma that acquired resistance to EGFR-tyrosine kinase inhibitors with T790M mutation and epithelial-to-mesenchymal transition
by: Nana Zhang, et al.
Published: (2017-01-01) -
Development of new mouse lung tumor models expressing EGFR T790M mutants associated with clinical resistance to kinase inhibitors.
by: Lucia Regales, et al.
Published: (2007-08-01)