Xinnan Li
639 Longmian Avenue
Nanjing, 211198, China
Nanjing, 211198, China
Last Updated: 09/26/2026
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Found 12 publications
Discovery of SY-589, a Highly Potent and Orally Bioavailable Polθ Helicase Inhibitor for the Treatment of HR-Deficient Tumors.
Journal: Journal of medicinal chemistry
Published: January 23, 2026
Targeting ClpP Protease: Emerging Therapeutic Strategies and Small-Molecule Modulators in Drug Discovery.
Journal: Medicinal research reviews
Published: December 02, 2025
Targeting RNA binding proteins with small-molecule inhibitors: Advances, challenges, and therapeutic opportunities.
Journal: Acta pharmaceutica Sinica. B
Published: May 19, 2025
Identification of 6-Fluorine-Substituted Coumarin Analogues as POLRMT Inhibitors with High Potency and Safety for Treatment of Pancreatic Cancer.
Journal: Journal of medicinal chemistry
Published: July 25, 2024
Design, Synthesis, and Biological Evaluation of Novel Tetrahydroacridin Hybrids with Sulfur-Inserted Linkers as Potential Multitarget Agents for Alzheimer's Disease.
Journal: Molecules (Basel, Switzerland)
Published: March 08, 2024
Design, synthesis and biological evaluation of novel indanones derivatives as potent acetylcholinesterase/monoamine oxidase B inhibitors.
Journal: Future medicinal chemistry
Published: October 30, 2023
Discovery of a Novel, Potent, Orally Active, and Safe Inhibitor Targeting Human Mitochondrial RNA Polymerase.
Journal: Journal of medicinal chemistry
Published: March 30, 2023
Design, Synthesis, and Biological Evaluation of Novel Chromanone Derivatives as Multifunctional Agents for the Treatment of Alzheimer's Disease.
Journal: ACS chemical neuroscience
Published: November 16, 2022
Novel and Potent Acetylcholinesterase Inhibitors for the Treatment of Alzheimer's Disease from Natural (±)-7,8-Dihydroxy-3-methyl-isochroman-4-one.
Journal: Molecules (Basel, Switzerland)
Published: April 12, 2022
Development of Alectinib-Based PROTACs as Novel Potent Degraders of Anaplastic Lymphoma Kinase (ALK).
Journal: Journal of medicinal chemistry
Published: June 28, 2021
Design, synthesis, biological evaluation, and docking study of 4-isochromanone hybrids bearing N-benzyl pyridinium moiety as dual binding site acetylcholinesterase inhibitors (part II).
Journal: Chemical biology & drug design
Published: August 05, 2017
Showing 1-12 of 12
Last Updated: 09/26/2026