Deyu Wu
State Key Laboratory Of Bioactive Substance And Function Of Natural Medicines, Chinese Academy Of Medical Sciences & Peking Union Medical College
Beijing, 100050, China
Beijing, 100050, China
Last Updated: 09/26/2026
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Found 18 publications
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
Catalyst-Controlled Switchable Mono-/Di-C-H Arylation of Aromatic Amides with Arylsilanes.
Journal: Organic letters
Published: September 20, 2025
Optimization of Thienopyrimidine Derivatives as Potent and Selective PI3Kδ Inhibitors for Cancer Immunotherapy.
Journal: Journal of medicinal chemistry
Published: July 15, 2025
Discovery and Optimization of Potent PROTAC Degraders of Phosphoinositide 3-Kinase with Significant in Vivo Anticancer Efficacy.
Journal: Journal of medicinal chemistry
Published: June 16, 2025
Design, synthesis and biological evaluation of a novel PSMA-PI3K small molecule drug conjugate.
Journal: RSC medicinal chemistry
Published: April 10, 2024
Design, Synthesis, and Bioevaluation of Novel Reversibly Photoswitchable PI3K Inhibitors Based on Phenylazopyridine Derivatives toward Light-Controlled Cancer Treatment.
Journal: Journal of medicinal chemistry
Published: February 20, 2024
Rational design and optimization of novel 4-methyl quinazoline derivatives as PI3K/HDAC dual inhibitors with benzamide as zinc binding moiety for the treatment of acute myeloid leukemia.
Journal: European journal of medicinal chemistry
Published: October 06, 2023
Optimization of Benzamide Derivatives as Potent and Orally Active Tubulin Inhibitors Targeting the Colchicine Binding Site.
Journal: Journal of medicinal chemistry
Published: December 13, 2022
Cp*CoIII-catalyzed formal [4 + 2] cycloaddition of 2-phenyl-1H-imidazoles to afford imidazo[1,2-c]quinazoline derivatives.
Journal: Organic & biomolecular chemistry
Published: June 13, 2022
Design and Optimization of Thienopyrimidine Derivatives as Potent and Selective PI3Kδ Inhibitors for the Treatment of B-Cell Malignancies.
Journal: Journal of medicinal chemistry
Published: May 24, 2022
Bioevaluation of a dual PI3K/HDAC inhibitor for the treatment of diffuse large B-cell lymphoma.
Journal: Bioorganic & medicinal chemistry letters
Published: May 04, 2022
Last Updated: 09/26/2026