Jianing Liao
State Key Laboratory Of Advanced Drug Delivery And Release Systems
Hangzhou, 310058, China
Hangzhou, 310058, China
Last Updated: 09/26/2026
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Found 10 publications
Discovery of N-(thiazol-2-yl) Furanamide Derivatives as Potent Orally Efficacious AR Antagonists with Low BBB Permeability.
Journal: Journal of medicinal chemistry
Published: September 10, 2025
Unraveling the Efficacy of AR Antagonists Bearing N-(4-(Benzyloxy)phenyl)piperidine-1-sulfonamide Scaffold in Prostate Cancer Therapy by Targeting LBP Mutations.
Journal: Journal of medicinal chemistry
Published: June 03, 2025
Corrigendum to "Discovery of novel tetrahydroquinoline derivatives as potent, selective, and orally Available AR antagonists" [Eur. J. Med. Chem. 291 (2025) 117566].
Journal: European journal of medicinal chemistry
Published: May 04, 2025
Discovery of N-(1,2,4-Thiadiazol-5-yl)benzo[b]oxepine-4-carboxamide Derivatives as Novel Antiresistance Androgen Receptor Antagonists.
Journal: Journal of medicinal chemistry
Published: January 23, 2025
Discovery of novel tetrahydroquinoline derivatives as potent, selective, and orally Available AR antagonists.
Journal: European journal of medicinal chemistry
Published: January 20, 2025
Discovery of 5-Nitro-N-(3-(trifluoromethyl)phenyl) Pyridin-2-amine as a Novel Pure Androgen Receptor Antagonist against Antiandrogen Resistance.
Journal: Journal of medicinal chemistry
Published: November 07, 2024
Identification of Oral Bioavailable Coumarin Derivatives as Potential AR Antagonists Targeting Prostate Cancer.
Journal: Journal of medicinal chemistry
Published: November 04, 2024
Discovery of Thiadiazoleamide Derivatives as Potent, Selective, and Orally Available Antagonists Disrupting Androgen Receptor Homodimer.
Journal: Journal of medicinal chemistry
Published: September 28, 2024
Small-Molecule Inhibition of Androgen Receptor Dimerization as a Strategy against Prostate Cancer.
Journal: ACS central science
Published: December 31, 2022
Discovery of a Novel Androgen Receptor Antagonist Manifesting Evidence to Disrupt the Dimerization of the Ligand-Binding Domain via Attenuating the Hydrogen-Bonding Network Between the Two Monomers.
Journal: Journal of medicinal chemistry
Published: November 23, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026