about
Pterostilbene Induces Cell Apoptosis and Cell Cycle Arrest in T-Cell Leukemia/Lymphoma by Suppressing the ERK1/2 Pathway.Combined Virtual Screening and Substructure Search for Discovery of Novel FABP4 Inhibitors.Rh(III)-catalyzed Redox-Neutral Unsymmetrical C-H Alkylation and Amidation Reactions of N-Phenoxyacetamides.How Well Can Implicit Solvent Simulations Explore Folding Pathways? A Quantitative Analysis of α-Helix Bundle Proteins.Transgelin-2 as a therapeutic target for asthmatic pulmonary resistance.Design, Synthesis and Pharmacological Evaluation of Novel Hsp90N-terminal Inhibitors Without Induction of Heat Shock ResponseMass Spectrometry and Theoretical Investigation of VN n+ ( n = 8, 9, and 10) ClustersMolecular Mechanism of Binding Selectivity of Inhibitors toward BACE1 and BACE2 Revealed by Multiple Short Molecular Dynamics Simulations and Free-Energy PredictionsPharmacokinetics-Driven Optimization of 4(3 H)-Pyrimidinones as Phosphodiesterase Type 5 Inhibitors Leading to TPN171, a Clinical Candidate for the Treatment of Pulmonary Arterial HypertensionD3Pockets: A Method and Web Server for Systematic Analysis of Protein Pocket DynamicsUnderestimated Noncovalent Interactions in Protein Data BankDiscovery of New and Potent InhA Inhibitors as Antituberculosis Agents: Structure-Based Virtual Screening Validated by Biological Assays and X-ray CrystallographyConformation of the Macrocyclic Drug Lorlatinib in Polar and Nonpolar Environments: A MD Simulation and NMR StudyHalogen bonding in differently charged complexes: basic profile, essential interaction terms and intrinsic σ-holeAccurate prediction of relative binding affinities of a series of HIV-1 protease inhibitors using semi-empirical quantum mechanical chargeNelfinavir was predicted to be a potential inhibitor of 2019-nCov main protease by an integrative approach combining homology modelling, molecular docking and binding free energy calculation
P50
Q41141664-BCC888FD-BE34-4390-851E-F22E00219427Q42798276-D4FB3C3F-CA21-48AA-8704-EF33E492B48BQ46259654-103BCC8F-9F67-499E-BA5D-4719294AE2B6Q47421641-2E928087-601C-4155-8B6F-8A68D1E78B8DQ50045900-8D99AD40-286D-4FB8-8DC4-07FF24FD406AQ64106380-C883271D-07D8-4579-961D-B31A3D576FA5Q88531122-63C16D23-1319-442D-BB25-C9853C1405C2Q90219593-AAD72085-716E-4EE2-B7BF-FAB6000C5FEEQ91506021-03BBFFF4-CA36-48D5-A692-9727FB1B5755Q91551261-1863D021-FDED-4B6D-AC59-325CFD9C83D7Q91794456-F3F47EAF-4FE5-45C5-A392-FE864B8E4EFCQ91840470-9E92A9CE-27E7-4236-BF3E-C3BD5539F851Q92347375-72D63710-00A6-4EC3-AFB3-456249F45755Q93037830-6B78974A-D840-4082-A69A-ED54FD579F18Q94466251-1B087F2E-9C39-43AF-A6C9-11AEFCB3E5E0Q95643368-3F389699-A951-4178-9272-F058BDA41F7E
P50
description
researcher
@en
name
Weiliang Zhu
@en
type
label
Weiliang Zhu
@en
prefLabel
Weiliang Zhu
@en
P31
P496
0000-0001-6699-5299