Deheng Sun
Suite 901, Changtai Plaza, 2889 Jinke Road
Pudong, 201203, China
Pudong, 201203, China
Last Updated: 09/26/2026
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Found 16 publications
Design, Synthesis and Biological Evaluation of Novel, Potent, Selective and Orally Available DGKα Inhibitors for the Treatment of Tumors.
Journal: Journal of medicinal chemistry
Published: December 01, 2025
Discovery of Novel, Potent, Selective, and Orally Available DGKα Inhibitors for the Treatment of Tumors.
Journal: Journal of medicinal chemistry
Published: September 08, 2025
Design and development of novel EGFR inhibitors spanning all subgroups of EGFR mutations in non-small cell lung cancer.
Journal: Innovation (Cambridge (Mass.))
Published: May 22, 2025
A novel, covalent broad-spectrum inhibitor targeting human coronavirus Mpro.
Journal: Nature communications
Published: March 04, 2025
Design, Synthesis, and Biological Evaluation of Novel Orally Available Covalent CDK12/13 Dual Inhibitors for the Treatment of Tumors.
Journal: Journal of medicinal chemistry
Published: February 14, 2025
Synthesis and structure-activity optimization of azepane-containing derivatives as PTPN2/PTPN1 inhibitors.
Journal: European journal of medicinal chemistry
Published: March 05, 2024
Discovery of 3-hydroxymethyl-azetidine derivatives as potent polymerase theta inhibitors.
Journal: Bioorganic & medicinal chemistry
Published: January 29, 2024
Discovery of Potent and Noncovalent Reversible EGFR Kinase Inhibitors of EGFRL858R/T790M/C797S.
Journal: ACS medicinal chemistry letters
Published: November 21, 2018
Design, Synthesis, and Biological Evaluation of Pyrimido[4,5- d]pyrimidine-2,4(1 H,3 H)-diones as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation.
Journal: Journal of medicinal chemistry
Published: June 16, 2018
Structure-Guided Design of C4-alkyl-1,4-dihydro-2H-pyrimido[4,5-d][1,3]oxazin-2-ones as Potent and Mutant-Selective Epidermal Growth Factor Receptor (EGFR) L858R/T790M Inhibitors.
Journal: Scientific reports
Published: August 30, 2016
Discovery and Structural Optimization of N5-Substituted 6,7-Dioxo-6,7-dihydropteridines as Potent and Selective Epidermal Growth Factor Receptor (EGFR) Inhibitors against L858R/T790M Resistance Mutation.
Journal: Journal of medicinal chemistry
Published: July 12, 2016
Last Updated: 09/26/2026