Zheng-chao Tu

State Key Laboratory Of Bioactive Molecules And Druggability Assessment
Guangzhou, 510632, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 46 publications

Rearranged phenylpropanoyl-phloroglucinol dimers from the flowers of Xanthostemon chrysanthus.

Rearranged phenylpropanoyl-phloroglucinol dimers from the flowers of Xanthostemon chrysanthus.

Journal: Phytochemistry

Published: February 25, 2026

Discovery and Biomimetic Syntheses of Phloroglucinol-Monoterpene-Triketone Hybrids from Chamelaucium uncinatum with Hypoglycemic Activity.

Discovery and Biomimetic Syntheses of Phloroglucinol-Monoterpene-Triketone Hybrids from Chamelaucium uncinatum with Hypoglycemic Activity.

Journal: Organic letters

Published: June 10, 2025

Novel spirooxindole alkaloid derivatives from the medicinal insect Blaps japanensis and their biological evaluation.

Novel spirooxindole alkaloid derivatives from the medicinal insect Blaps japanensis and their biological evaluation.

Journal: Bioorganic chemistry

Published: July 10, 2023

Eugenilones A-N: sesquiterpenoids from the fruits of Eugenia uniflora.

Eugenilones A-N: sesquiterpenoids from the fruits of Eugenia uniflora.

Journal: Phytochemistry

Published: February 21, 2023

Discovery of AXL Degraders with Improved Potencies in Triple-Negative Breast Cancer (TNBC) Cells.

Discovery of AXL Degraders with Improved Potencies in Triple-Negative Breast Cancer (TNBC) Cells.

Journal: Journal of medicinal chemistry

Published: January 25, 2023

1-Methyl-3-((4-(quinolin-4-yloxy)phenyl)amino)-1H-pyrazole-4-carboxamide derivatives as new rearranged during Transfection (RET) kinase inhibitors capable of suppressing resistant mutants in solvent-front regions.

1-Methyl-3-((4-(quinolin-4-yloxy)phenyl)amino)-1H-pyrazole-4-carboxamide derivatives as new rearranged during Transfection (RET) kinase inhibitors capable of suppressing resistant mutants in solvent-front regions.

Journal: European journal of medicinal chemistry

Published: July 06, 2022

Design, Synthesis, and Biological Evaluation of 2-Formyl Tetrahydronaphthyridine Urea Derivatives as New Selective Covalently Reversible FGFR4 Inhibitors.

Design, Synthesis, and Biological Evaluation of 2-Formyl Tetrahydronaphthyridine Urea Derivatives as New Selective Covalently Reversible FGFR4 Inhibitors.

Journal: Journal of medicinal chemistry

Published: February 04, 2022

Investigation of Covalent Warheads in the Design of 2-Aminopyrimidine-based FGFR4 Inhibitors.

Investigation of Covalent Warheads in the Design of 2-Aminopyrimidine-based FGFR4 Inhibitors.

Journal: ACS medicinal chemistry letters

Published: January 23, 2021

Neolignans and Norlignans from Insect Medicine Polyphaga plancyi and Their Biological Activities.

Neolignans and Norlignans from Insect Medicine Polyphaga plancyi and Their Biological Activities.

Journal: Natural products and bioprospecting

Published: July 03, 2020

Sulfur and nitrogen-containing compounds from the whole bodies of Blaps japanensis.

Sulfur and nitrogen-containing compounds from the whole bodies of Blaps japanensis.

Journal: Bioorganic chemistry

Published: May 06, 2020

Design, synthesis, and Structure-Activity Relationships (SAR) of 3-vinylindazole derivatives as new selective tropomyosin receptor kinases (Trk) inhibitors.

Design, synthesis, and Structure-Activity Relationships (SAR) of 3-vinylindazole derivatives as new selective tropomyosin receptor kinases (Trk) inhibitors.

Journal: European journal of medicinal chemistry

Published: April 01, 2020

Ansamycin derivatives from the marine-derived Streptomyces sp. SCSGAA 0027 and their cytotoxic and antiviral activities.

Ansamycin derivatives from the marine-derived Streptomyces sp. SCSGAA 0027 and their cytotoxic and antiviral activities.

Journal: Bioorganic & medicinal chemistry letters

Published: February 27, 2020

Showing 1-12 of 46

Last Updated: 09/26/2026