Jiaying Xiong
Liuzhou, 545005, China
Last Updated: 09/26/2026
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Found 16 publications
Design and synthesis of long-acting prodrugs of SEP-363856 with sustained antipsychotic-like activity.
Journal: Bioorganic chemistry
Published: June 16, 2026
Discovery of novel N-(alkylpiperidinyl) substituted benzamides targeting the glycine transporter 2 with anti-nociceptive effects in neuropathic pain.
Journal: European journal of medicinal chemistry
Published: April 10, 2026
Targeting P2X receptors for analgesia: Small molecule antagonists in development.
Journal: European journal of medicinal chemistry
Published: April 08, 2026
Etomidate derivatives: fine-tuning of molecular structure and innovation in pharmacological effects.
Etomidate derivatives: fine-tuning of molecular structure and innovation in pharmacological effects.
Journal: European journal of medicinal chemistry
Published: February 14, 2026
MC4R Antagonists: A Promising New Hope for the Treatment of Cachexia and Wasting Diseases.
Journal: Die Pharmazie
Published: December 09, 2025
A photo-elutable 8-17 DNAzyme labeling and PCR-free colorimetric quantification strategy for 5-hydroxymethylcytosine in mammalian genomic DNA.
Journal: Analytical methods : advancing methods and applications
Published: February 10, 2025
Discovery of a novel KV7.2/7.3 channels agonist for the treatment of neuropathic pain.
Journal: European journal of medicinal chemistry
Published: August 02, 2024
Benzylaminofentanyl derivates: Discovery of bifunctional μ opioid and σ1 receptor ligands as novel analgesics with reduced adverse effects.
Journal: European journal of medicinal chemistry
Published: March 28, 2022
The Potential Antidepressant Action of Duloxetine Co-Administered with the TAAR1 Receptor Agonist SEP-363856 in Mice.
Journal: Molecules (Basel, Switzerland)
Published: February 11, 2022
Optimization of bifunctional piperidinamide derivatives as σ1R Antagonists/MOR agonists for treating neuropathic pain.
Journal: European journal of medicinal chemistry
Published: July 17, 2021
Bifunctional μ opioid and σ1 receptor ligands as novel analgesics with reduced side effects.
Journal: European journal of medicinal chemistry
Published: April 14, 2021
Design, Synthesis and Biological Investigation of Flavone Derivatives as Potential Multi-Receptor Atypical Antipsychotics.
Journal: Molecules (Basel, Switzerland)
Published: August 17, 2020
Last Updated: 09/26/2026