Guo Zhang
Cancer Center And State Key Laboratory Of Biotherapy
Chengdu, China
Chengdu, China
Last Updated: 09/26/2026
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Found 20 publications
Discovery of a Potent and Selective Cell-Active Inhibitor of Histidine-N1 Methyltransferase METTL9.
Journal: Angewandte Chemie (International ed. in English)
Published: January 16, 2026
Discovery of 4-((quinolin-8-ylthio)methyl)benzamide derivatives as a new class of SARS-CoV-2 nsp13 inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: January 27, 2025
An orally available Mpro/TMPRSS2 bispecific inhibitor with potent anti-coronavirus efficacy in vivo.
An orally available Mpro/TMPRSS2 bispecific inhibitor with potent anti-coronavirus efficacy in vivo.
Journal: Research square
Published: November 28, 2024
A deep learning model for structure-based bioactivity optimization and its application in the bioactivity optimization of a SARS-CoV-2 main protease inhibitor.
Journal: European journal of medicinal chemistry
Published: November 19, 2024
An orally available Mpro/TMPRSS2 bispecific inhibitor with potent anti-coronavirus efficacy in vivo.
An orally available Mpro/TMPRSS2 bispecific inhibitor with potent anti-coronavirus efficacy in vivo.
Journal: Nature communications
Published: November 14, 2024
Cloud computing convergence: integrating computer applications and information management for enhanced efficiency.
Journal: Frontiers in big data
Published: October 08, 2024
Discovery of 5-((1H-indazol-3-yl) methylene)-2-thioxoimidazolidin-4-one derivatives as a new class of AHR agonists with anti-psoriasis activity in a mouse model.
Journal: Bioorganic & medicinal chemistry letters
Published: May 21, 2023
Discovery of 3-phenyl-1,2,4-oxadiazole derivatives as a new class of SARS-CoV-2 main protease inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: December 19, 2022
Non-classical ferroptosis inhibition by a small molecule targeting PHB2.
Journal: Nature communications
Published: May 24, 2022
Discovery of 2-vinyl-10H-phenothiazine derivatives as a class of ferroptosis inhibitors with minimal human Ether-a-go-go related gene (hERG) activity for the treatment of DOX-induced cardiomyopathy.
Journal: Bioorganic & medicinal chemistry letters
Published: April 13, 2022
Identification of triazolopyridine derivatives as a new class of AhR agonists and evaluation of anti-psoriasis effect in a mouse model.
Journal: European journal of medicinal chemistry
Published: November 09, 2021
Last Updated: 09/26/2026