Hong-bo Wang
Key Laboratory Of Molecular Pharmacology And Drug Evaluation
Yantai, 264005, China
Yantai, 264005, China
Last Updated: 09/26/2026
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Found 30 publications
Dual BRD4/AKT inhibition overcomes c-MYC-driven resistance in metastatic castration-resistant prostate cancer.
Journal: European journal of medicinal chemistry
Published: February 12, 2026
Inhibition of the ATR-DNAPKcs-RB axis drives G1/S-phase transition and sensitizes triple-negative breast cancer (TNBC) to DNA holliday junctions.
Journal: Biochemical pharmacology
Published: February 05, 2024
A novel role for microtubule affinity-regulating kinases in neuropathic pain.
Journal: British journal of pharmacology
Published: August 03, 2023
Synthesis and evaluation of piperazinotriazoles. Discovery of a potent and orally bioavailable neurokinin-3 receptor inhibitor.
Journal: European journal of medicinal chemistry
Published: April 03, 2023
Reproductive and developmental toxicity assessments of LPM3480392, a novel mu opioid receptor biased agonist in rats.
Journal: Reproductive toxicology (Elmsford, N.Y.)
Published: March 24, 2023
Chronic Stress-Induced Elevation of Melanin-Concentrating Hormone in the Locus Coeruleus Inhibits Norepinephrine Production and Associated With Depression-Like Behaviors in Rats.
Journal: The international journal of neuropsychopharmacology
Published: January 21, 2023
Identification of a novel heterogeneous nuclear ribonucleoprotein A2B1 (hnRNPA2B1) ligand that disrupts HnRNPA2B1/nucleic acid interactions to inhibit the MDMX-p53 axis in gastric cancer.
Journal: Pharmacological research
Published: December 14, 2022
Synthesis, biological, and structural explorations of a series of μ-opioid receptor (MOR) agonists with high G protein signaling bias.
Journal: European journal of medicinal chemistry
Published: October 08, 2021
VE-822, a novel DNA Holliday junction stabilizer, inhibits homologous recombination repair and triggers DNA damage response in osteogenic sarcomas.
Journal: Biochemical pharmacology
Published: June 30, 2021
mTOR regulates cocaine-induced behavioural sensitization through the SynDIG1-GluA2 interaction in the nucleus accumbens.
Journal: Acta pharmacologica Sinica
Published: April 10, 2021
Metabolomics, metabolic flux analysis and cancer pharmacology.
Journal: Pharmacology & therapeutics
Published: January 03, 2021
Natural product 1,2,3,4,6-penta-O-galloyl-β-D-glucopyranose is a reversible inhibitor of glyceraldehyde 3-phosphate dehydrogenase.
Journal: Acta pharmacologica Sinica
Published: December 17, 2020
Last Updated: 09/26/2026