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Covalent fragment libraries in drug discovery - ScienceDirect
DeepConv-DTI: Prediction of drug-target interactions via deep learning with convolution on protein sequences
Recent advances in combinatorial drug screening and synergy scoring - ScienceDirect
Covalent fragment libraries in drug discovery - ScienceDirect
The nature of ligand efficiency | SpringerLink
The impact of early ADME profiling on drug discovery and development strategy - Drug Discovery World (DDW)
Recent advances in combinatorial drug screening and synergy scoring - ScienceDirect
The implications of target saturation for the use of drug–target residence time | Nature Reviews Drug Discovery
Biased Receptor Signaling in Drug Discovery | Pharmacological Reviews
Creating and screening natural product libraries - Natural Product Reports (RSC Publishing) DOI:10.1039/C9NP00068B
PDF) Theoretical Basis, Experimental Design, and Computerized Simulation of Synergism and Antagonism in Drug Combination Studies
A Comprehensive Biophysical Analysis of the Effect of DNA Binding Drugs on Protamine-induced DNA Condensation | Scientific Reports
The drug–target residence time model: a 10-year retrospective | Nature Reviews Drug Discovery
Covalent fragment libraries in drug discovery - ScienceDirect
Investigating antimalarial drug interactions of emetine dihydrochloride hydrate using CalcuSyn-based interactivity calculations
Covalent fragment libraries in drug discovery - ScienceDirect
Investigating antimalarial drug interactions of emetine dihydrochloride hydrate using CalcuSyn-based interactivity calculations
Drug design from the cryptic inhibitor envelope | Nature Communications
Automating drug discovery | Nature Reviews Drug Discovery
Organ‐on‐chip models: Implications in drug discovery and clinical applications - Mittal - 2019 - Journal of Cellular Physiology - Wiley Online Library
Automating drug discovery | Nature Reviews Drug Discovery
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