Baolian O. Wang
Beijing Key Laboratory Of Active Substances Discovery And Druggability Evaluation, Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, 100050, China
Beijing, 100050, China
Last Updated: 09/26/2026
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Found 50 publications
Discovery of 1H-Indole-3-Propionamide Derivatives as Potent, Selective and Orally Available NaV1.7 Inhibitors for Pain Treatment.
Journal: Journal of medicinal chemistry
Published: July 27, 2026
Discovery and Optimization of 4-Methylquinazoline Derivatives as Highly Selective PI3Kδ Inhibitors for the Treatment of Acute Lung Injury.
Journal: Journal of medicinal chemistry
Published: May 24, 2026
Discovery of Potent Benzoselenazinone-Based DprE1 Inhibitors: A Novel Selenium-Containing Scaffold with Superior Anti-TB Activity and Pharmacokinetic Properties.
Journal: Journal of medicinal chemistry
Published: April 17, 2026
Structure-enabled discovery of carboxylate esters prodrugs as potential potent inhibitors targeting Glutaminase C.
Journal: Bioorganic chemistry
Published: September 28, 2025
One-Shot Rational Design of Covalent Drugs with CovalentLab.
Journal: JACS Au
Published: September 05, 2025
Deep learning-based discovery of tetrahydrocarbazoles as broad-spectrum antitumor agents and click-activated strategy for targeted cancer therapy.
Journal: Acta pharmaceutica Sinica. B
Published: March 04, 2025
Saorilao Qingfei Zhike Capsule alleviated inflammation and bronchial remodeling in LPS and CS-induced COPD via MAPK signaling pathway.
Journal: Journal of ethnopharmacology
Published: March 02, 2025
Pharmacokinetics and related gender difference studies of four active components of Codonopsis Pilosula by LC-MS/MS determination.
Journal: Journal of ethnopharmacology
Published: July 15, 2024
Bioequivalence Analysis of Terazosin Hydrochloride Tablets Based on Parallel Artificial Membrane Permeability Analysis.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: June 15, 2024
Design, Synthesis, and Biological Evaluation of 1,2,4-Oxadiazole Derivatives Containing an Aryl Carboxylic Acid Moiety as Potent Sarbecovirus Papain-like Protease Inhibitors.
Journal: Journal of medicinal chemistry
Published: June 13, 2024
Identification of a novel xanthine oxidoreductase inhibitor for hyperuricemia treatment with high efficacy and safety profile.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: May 23, 2024
Last Updated: 09/26/2026