Liqian Gao

135 Xingang Xi Road
Guangzhou, 510275, China

Last Updated: 09/26/2026

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Found 43 publications

Large-Scale Profiling of Kinase Degradation by Using Norbornene-Based Hydrophobic Tag (HyT) Strategy.

Large-Scale Profiling of Kinase Degradation by Using Norbornene-Based Hydrophobic Tag (HyT) Strategy.

Journal: Angewandte Chemie (International ed. in English)

Published: December 18, 2025

Cell-Active, Arginine-Targeting Irreversible Covalent Inhibitors for Non-Kinases and Kinases.

Cell-Active, Arginine-Targeting Irreversible Covalent Inhibitors for Non-Kinases and Kinases.

Journal: Angewandte Chemie (International ed. in English)

Published: November 17, 2024

KAHA ligation as a platform for the rapid discovery of Protein Tyrosine phosphatase 1B (PTP1B) inhibitors.

KAHA ligation as a platform for the rapid discovery of Protein Tyrosine phosphatase 1B (PTP1B) inhibitors.

Journal: Bioorganic chemistry

Published: September 15, 2024

Rationally designed BCR-ABL kinase inhibitors for improved leukemia treatment via covalent and pro-/dual-drug targeting strategies.

Rationally designed BCR-ABL kinase inhibitors for improved leukemia treatment via covalent and pro-/dual-drug targeting strategies.

Journal: Journal of advanced research

Published: June 28, 2024

Kinase Inhibition via Small Molecule-Induced Intramolecular Protein Cross-Linking.

Kinase Inhibition via Small Molecule-Induced Intramolecular Protein Cross-Linking.

Journal: Angewandte Chemie (International ed. in English)

Published: February 29, 2024

Inhibition of HSP90 distinctively modulates the global phosphoproteome of Leishmania mexicana developmental stages.

Inhibition of HSP90 distinctively modulates the global phosphoproteome of Leishmania mexicana developmental stages.

Journal: Microbiology spectrum

Published: October 31, 2023

Global Reactivity Profiling of the Catalytic Lysine in Human Kinome for Covalent Inhibitor Development.

Global Reactivity Profiling of the Catalytic Lysine in Human Kinome for Covalent Inhibitor Development.

Journal: Angewandte Chemie (International ed. in English)

Published: October 30, 2023

Multitarget inhibitors/probes that target LRRK2 and AURORA A kinases noncovalently and covalently.

Multitarget inhibitors/probes that target LRRK2 and AURORA A kinases noncovalently and covalently.

Journal: Chemical communications (Cambridge, England)

Published: August 18, 2023

Meso-aryltellurium-BODIPY-based fluorescence turn-on probe for selective, sensitive and fast glutathione sensing in HepG2 cells.

Meso-aryltellurium-BODIPY-based fluorescence turn-on probe for selective, sensitive and fast glutathione sensing in HepG2 cells.

Journal: Talanta

Published: August 03, 2023

Cell-active, irreversible covalent inhibitors that selectively target the catalytic lysine of EGFR by using fluorosulfate-based SuFEx chemistry.

Cell-active, irreversible covalent inhibitors that selectively target the catalytic lysine of EGFR by using fluorosulfate-based SuFEx chemistry.

Journal: European journal of medicinal chemistry

Published: May 18, 2023

Mesopore-encaged active MnOx in nano-silica selectively suppresses lung cancer cells by inducing autophagy.

Mesopore-encaged active MnOx in nano-silica selectively suppresses lung cancer cells by inducing autophagy.

Journal: Biomaterials science

Published: February 01, 2023

Amplifying the efficacy of ALA-based prodrugs for photodynamic therapy using nanotechnology.

Amplifying the efficacy of ALA-based prodrugs for photodynamic therapy using nanotechnology.

Journal: Frontiers in pharmacology

Published: January 04, 2023

Showing 1-12 of 43

Last Updated: 09/26/2026