Cai-guang G. Yang
State Key Laboratory Of Drug Research
Shanghai, China
Shanghai, China
Last Updated: 09/26/2026
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Found 87 publications
Structure-Based Design of a Highly Potent Dual-Competitive FTO Inhibitor for Targeted m6A Demethylase Inhibition in AML.
Journal: Journal of medicinal chemistry
Published: November 05, 2025
Mitochondrial ClpX Inhibition Induces Ferroptosis and Blocks Pancreatic Cancer Cell Proliferation.
Journal: Chembiochem : a European journal of chemical biology
Published: July 21, 2025
Development of Orally Bioavailable FTO Inhibitors with Potent Antileukemia Efficacy.
Journal: Journal of medicinal chemistry
Published: June 28, 2025
Modular Synthesis of the Potent Antibiotic Amycolamicin and Diastereomeric Analogues Thereof.
Journal: Organic letters
Published: April 02, 2025
A patenting perspective of fat mass and obesity associated protein (FTO) inhibitors: 2017-present.
Journal: Expert opinion on therapeutic patents
Published: March 07, 2025
Structure-Based Development of a Covalent Inhibitor Targeting Streptococcus Pyogenes over Staphylococcus Aureus Sortase A.
Journal: Chemistry (Weinheim an der Bergstrasse, Germany)
Published: February 11, 2025
Discovery of Novel RNA Demethylase FTO Inhibitors Featuring an Acylhydrazone Scaffold with Potent Antileukemia Activity.
Journal: Journal of medicinal chemistry
Published: January 17, 2025
Development of 3-arylaminothiophenic-2-carboxylic acid derivatives as new FTO inhibitors showing potent antileukemia activities.
Journal: European journal of medicinal chemistry
Published: January 16, 2025
Applying natural product repurposing strategy to identify baicalein as novel caseinolytic protease P inhibitor and its application in the treatment of rice bacterial diseases.
Journal: Pesticide biochemistry and physiology
Published: January 08, 2025
Structure-Guided Development of ClpP Agonists with Potent Therapeutic Activities against Staphylococcus aureus Infection.
Journal: Journal of medicinal chemistry
Published: January 06, 2025
Discovery of novel seven-membered ring derivatives of ONC212 as caseinolytic protease P protein activators using the ring expansion strategy: Rational design, synthesis, and antibacterial evaluation.
Journal: International journal of biological macromolecules
Published: December 26, 2024
Last Updated: 09/26/2026