Huihao M. Zhou
132 East Outer Ring Road
Guangzhou, 510006, China
Guangzhou, 510006, China
Last Updated: 09/26/2026
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Found 90 publications
Crystallographic analysis of a putative FAD-dependent oxidoreductase identifies a potentially misfolded apo structure in a soluble monomeric state.
Journal: Journal of structural biology
Published: February 28, 2026
Substrate l-isoleucine facilitates the hyper inhibition of reveromycin A on human cytoplasmic isoleucyl-tRNA synthetase.
Journal: Archives of biochemistry and biophysics
Published: November 04, 2025
Discovery of a triple-site inhibitor targeting bacterial methionyl-tRNA synthetase through combined drug repurposing screening and generative AI-assisted optimization.
Journal: Nucleic acids research
Published: September 30, 2025
Optimization of Novel Quinazolines as Potent Aurora Kinase Inhibitors for Triple-Negative Breast Cancer Treatment.
Journal: Journal of medicinal chemistry
Published: August 25, 2025
The Structure of Carboxyl Methyltransferase Provides Insights Into the Substrate Specificity and Divergent Evolution of Iridoid.
Journal: Plant biotechnology journal
Published: June 22, 2025
Phase separation of RXRγ drives tumor chemoresistance and represents a therapeutic target for small-cell lung cancer.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: May 20, 2025
RORγ Hijacks HIF1α to Promote Peritoneal Metastasis of Gastric Cancer.
Journal: Cancer research
Published: April 18, 2025
Development of potent inhibitors targeting bacterial prolyl-tRNA synthetase through fluorine scanning-directed activity tuning.
Journal: European journal of medicinal chemistry
Published: February 20, 2025
UMP functions as an endogenous regulator of NR4A1 to control gastric cancer progression.
Journal: Molecular cell
Published: December 03, 2024
Structure-guided inhibitor design targeting CntL provides the first chemical validation of the staphylopine metallophore system in bacterial metal acquisition.
Journal: European journal of medicinal chemistry
Published: September 28, 2024
Discovery of Novel Neo-Clerodane Derivatives as Potent Dual-Functional Antiosteoporosis Agents through Targeting Peroxisome Proliferator-Activated Receptor-γ.
Journal: Journal of medicinal chemistry
Published: August 26, 2024
Last Updated: 09/26/2026