Hong-yi Zhao
Shaanxi 710061, PR China
Puerto Rico
Puerto Rico
Last Updated: 09/26/2026
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Found 24 publications
Synthesis and degradation effect of PROTACs targeting EGFR triple mutants.
Journal: Bioorganic & medicinal chemistry
Published: August 19, 2025
Lysine-Targeted Covalent Strategy Leading to the Discovery of Novel Potent PROTAC-Based PI3Kδ Degraders.
Journal: Journal of medicinal chemistry
Published: May 31, 2025
EGFR tyrosine kinase inhibitor ZZC4 overcomes acquired resistance to gefitinib.
Journal: Toxicology and applied pharmacology
Published: December 02, 2024
Lysine-Targeted Covalent Inhibitors of PI3Kδ Synthesis and Screening by In Situ Interaction Upgradation.
Journal: Journal of medicinal chemistry
Published: November 19, 2024
Modification of osimertinib to discover new potent EGFRC797S-TK inhibitors.
Journal: European journal of medicinal chemistry
Published: August 29, 2023
Design, synthesis and evaluation of new pyrimidine derivatives as EGFRC797S tyrosine kinase inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: May 06, 2023
Discovery of Novel, Potent, and Selective Small-Molecule Menin-Mixed Lineage Leukemia Interaction Inhibitors through Attempting Introduction of Hydrophilic Groups.
Journal: Journal of medicinal chemistry
Published: September 29, 2022
Progress of small molecules for targeted protein degradation: PROTACs and other technologies.
Journal: Drug development research
Published: September 11, 2022
Overcoming C797S mutation: The challenges and prospects of the fourth-generation EGFR-TKIs.
Journal: Bioorganic chemistry
Published: April 22, 2022
Discovery of Potent PROTACs Targeting EGFR Mutants through the Optimization of Covalent EGFR Ligands.
Journal: Journal of medicinal chemistry
Published: March 07, 2022
Identification of benzamides derivatives of norfloxacin as promising microRNA-21 inhibitors via repressing its transcription.
Journal: Bioorganic & medicinal chemistry
Published: January 11, 2022
Last Updated: 09/26/2026