Weige Zhang
Wenhua Road 103
Shenyang, 110016, China
Shenyang, 110016, China
Last Updated: 09/26/2026
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Found 28 publications
Design, synthesis, and bioevaluation of pyrazole-containing tubulin polymerisation inhibitors based on conformational constraint strategy.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: September 23, 2025
A Dual-Mechanism Targeted Cross-Convergence Prodrug Activation Strategy Enabled by Biological Stimulus Amplification toward Precision Cancer Therapy.
Journal: Biomaterials research
Published: September 10, 2025
The ADAM17 inhibitor ZLDI-8 sensitized hepatocellular carcinoma cells to sorafenib through Notch1-integrin β-talk.
Journal: Pharmacological research
Published: October 25, 2023
Design, synthesis, and biological evaluation of biotinylated colchicine derivatives as potential antitumor agents.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: December 17, 2021
Survivin suppression heightens BZML-induced mitotic catastrophe to overcome multidrug resistance by removing therapy-induced senescent A549/Taxol cells.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: May 25, 2021
2-Methoxy-5((3,4,5-trimethosyphenyl) seleninyl) phenol causes G2/M cell cycle arrest and apoptosis in NSCLC cells through mitochondrial apoptotic pathway and MDM2 inhibition.
Journal: Journal of biochemical and molecular toxicology
Published: May 09, 2021
Design, synthesis and biological evaluation of 1-Aryl-5-(4-arylpiperazine-1-carbonyl)-1H-tetrazols as novel microtubule destabilizers.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: February 01, 2021
W436, a novel SMART derivative, exhibits anti-hepatocarcinoma activity by inducing apoptosis and G2/M cell cycle arrest in vitro and in vivo and induces protective autophagy.
Journal: Journal of biochemical and molecular toxicology
Published: November 30, 2020
YAN, a novel microtubule inhibitor, inhibits P-gp and MRP1 function and induces mitotic slippage followed by apoptosis in multidrug-resistant A549/Taxol cells.
Journal: Toxicology in vitro : an international journal published in association with BIBRA
Published: May 14, 2020
5-(3,4,5-trimethoxybenzoyl)-4-methyl-2-(p-tolyl) imidazol (BZML) targets tubulin and DNA to induce anticancer activity and overcome multidrug resistance in colorectal cancer cells.
Journal: Chemico-biological interactions
Published: September 03, 2019
2-Methoxy-5((3,4,5-trimethosyphenyl)seleninyl) phenol reverses EGF-induced cell migration and invasion through down-regulation of MDM2 in breast cancer cell lines.
Journal: Cancer biology & therapy
Published: December 06, 2018
Conformation impacts on the bioactivities of SMART analogues.
Journal: European journal of medicinal chemistry
Published: April 29, 2018
Last Updated: 09/26/2026