Matteo Masetti

Orcid: 0000-0002-3757-7802

According to our database1, Matteo Masetti authored at least 13 papers between 2008 and 2024.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of five.

Timeline

Legend:

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Bibliography

2024
Similarities and Differences in Ligand Binding to Protein and RNA Targets: The Case of Riboflavin.
J. Chem. Inf. Model., 2024

2023
Integrated Approach Including Docking, MD Simulations, and Network Analysis Highlights the Action Mechanism of the Cardiac hERG Activator RPR260243.
J. Chem. Inf. Model., August, 2023

2021
Targeting the JAK/STAT Pathway: A Combined Ligand- and Target-Based Approach.
J. Chem. Inf. Model., 2021

2020
Conduction and Gating Properties of the TRAAK Channel from Molecular Dynamics Simulations with Different Force Fields.
J. Chem. Inf. Model., 2020

Exploring Conformational Dynamics of the Extracellular Venus flytrap Domain of the GABAB Receptor: A Path-Metadynamics Study.
J. Chem. Inf. Model., 2020

2019
Predicting Residence Time and Drug Unbinding Pathway through Scaled Molecular Dynamics.
J. Chem. Inf. Model., 2019

2018
Fully Flexible Docking via Reaction-Coordinate-Independent Molecular Dynamics Simulations.
J. Chem. Inf. Model., 2018

Binding Residence Time through Scaled Molecular Dynamics: A Prospective Application to hDAAO Inhibitors.
J. Chem. Inf. Model., 2018

2017
Development of a multisite model for Ni(II) ion in solution from thermodynamic and kinetic data.
J. Comput. Chem., 2017

2013
An Automated Docking Protocol for hERG Channel Blockers.
J. Chem. Inf. Model., 2013

Collecting and Assessing Human Lactate Dehydrogenase-A Conformations for Structure-Based Virtual Screening.
J. Chem. Inf. Model., 2013

2012
Combining Dyad Protonation and Active Site Plasticity in BACE-1 Structure-Based Drug Design.
J. Chem. Inf. Model., 2012

2008
Modeling the hERG potassium channel in a phospholipid bilayer: Molecular dynamics and drug docking studies.
J. Comput. Chem., 2008


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