Shang Li

Jiangsu Key Laboratory Of Bioactive Natural Product Research And State Key Laboratory Of Natural Medicines
Nanjing, 210009, China

Last Updated: 09/26/2026

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Found 27 publications

Correction to "Discovery of Dual CDK6/BRD4 Inhibitor Inducing Apoptosis and Increasing the Sensitivity of Ferroptosis in Triple-Negative Breast Cancer".

Correction to "Discovery of Dual CDK6/BRD4 Inhibitor Inducing Apoptosis and Increasing the Sensitivity of Ferroptosis in Triple-Negative Breast Cancer".

Journal: Journal of medicinal chemistry

Published: January 28, 2025

Discovery of Dual CDK6/BRD4 Inhibitor Inducing Apoptosis and Increasing the Sensitivity of Ferroptosis in Triple-Negative Breast Cancer.

Discovery of Dual CDK6/BRD4 Inhibitor Inducing Apoptosis and Increasing the Sensitivity of Ferroptosis in Triple-Negative Breast Cancer.

Journal: Journal of medicinal chemistry

Published: November 22, 2024

Polypharmacological Drug Design Guided by Integrating Phenotypic and Restricted Fragment Docking Strategies.

Polypharmacological Drug Design Guided by Integrating Phenotypic and Restricted Fragment Docking Strategies.

Journal: Journal of medicinal chemistry

Published: September 19, 2024

Discovery of Covalent MLKL PROTAC Degraders via Optimization of a Theophylline Derivative Ligand for Treating Necroptosis.

Discovery of Covalent MLKL PROTAC Degraders via Optimization of a Theophylline Derivative Ligand for Treating Necroptosis.

Journal: Journal of medicinal chemistry

Published: August 24, 2024

Improving tumor sensitivity by the introduction of an ester chain to triaryl derivatives targeting PD-1/PD-L1.

Improving tumor sensitivity by the introduction of an ester chain to triaryl derivatives targeting PD-1/PD-L1.

Journal: European journal of medicinal chemistry

Published: March 26, 2024

Regioselective Olefination and Arylation of Arene-Tethered Diols Using the Easily Foldable Directing Groups.

Regioselective Olefination and Arylation of Arene-Tethered Diols Using the Easily Foldable Directing Groups.

Journal: Organic letters

Published: February 13, 2024

Dual target PARP1/EZH2 inhibitors inducing excessive autophagy and producing synthetic lethality for triple-negative breast cancer therapy.

Dual target PARP1/EZH2 inhibitors inducing excessive autophagy and producing synthetic lethality for triple-negative breast cancer therapy.

Journal: European journal of medicinal chemistry

Published: October 05, 2023

Indirubin derivatives as bifunctional molecules inducing DNA damage and targeting PARP for the treatment of cancer.

Indirubin derivatives as bifunctional molecules inducing DNA damage and targeting PARP for the treatment of cancer.

Journal: European journal of medicinal chemistry

Published: July 13, 2023

Design, synthesis and mechanism studies of dual EZH2/BRD4 inhibitors for cancer therapy.

Design, synthesis and mechanism studies of dual EZH2/BRD4 inhibitors for cancer therapy.

Journal: Bioorganic & medicinal chemistry

Published: April 27, 2023

Design and synthesis of antiviral pseudo-natural products through effective one-step acylmethylation macrocyclization.

Design and synthesis of antiviral pseudo-natural products through effective one-step acylmethylation macrocyclization.

Journal: Chinese journal of natural medicines

Published: March 12, 2023

Oxazole-4-carboxamide/butylated hydroxytoluene hybrids with GSK-3β inhibitory and neuroprotective activities against Alzheimer's disease.

Oxazole-4-carboxamide/butylated hydroxytoluene hybrids with GSK-3β inhibitory and neuroprotective activities against Alzheimer's disease.

Journal: European journal of medicinal chemistry

Published: February 24, 2023

Discovery of Sibiriline derivatives as novel receptor-interacting protein kinase 1 inhibitors.

Discovery of Sibiriline derivatives as novel receptor-interacting protein kinase 1 inhibitors.

Journal: European journal of medicinal chemistry

Published: December 20, 2022

Showing 1-12 of 27

Last Updated: 09/26/2026