Dahong Li
Key Laboratory Of Structure Based Drug Design & Discovery, 103 Wenhua Road, Shenyang 110016, PR China
Puerto Rico
Puerto Rico
Last Updated: 09/26/2026
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Found 12 publications
Corrigendum to "Thiol esters as chemical warheads of SARS-CoV-2 main protease (3CLpro) peptide-like inhibitors" [Eur. J. Med. Chem. 293 (2025) 117709].
Journal: European journal of medicinal chemistry
Published: December 10, 2025
An H₂S-releasing oridonin derivative protects HaCaT cells against metabolic stress via PI3K/AKT/Nrf2 signaling.
Journal: Molecular immunology
Published: September 03, 2025
Enhancement of anticancer potential of novel β-carboline derivatives by ACS81 hybridization.
Journal: Bioorganic & medicinal chemistry letters
Published: August 09, 2025
Corilagin regulates antigen processing and presentation by directly binding to inhibit ERAP1.
Journal: International immunopharmacology
Published: December 30, 2024
H2S-releasing oridonin derivatives with improved antitumor activity by inhibiting the PI3K/AKT pathway.
Journal: Bioorganic & medicinal chemistry
Published: September 04, 2024
Design and synthesis of 6,20-epoxy A-ring modified oridonin derivatives with antitumor activity through extrinsic and mitochondrial pathways.
Journal: Bioorganic chemistry
Published: May 05, 2024
Design and synthesis of chromone-nitrogen mustard derivatives and evaluation of anti-breast cancer activity.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: December 27, 2021
Small-molecule probes for fluorescent detection of cellular hypoxia-related nitroreductase.
Journal: Journal of pharmaceutical and biomedical analysis
Published: January 17, 2021
Effective enmein-type mimics of clinical candidate HAO472: Design, synthesis and biological evaluation.
Journal: European journal of medicinal chemistry
Published: January 23, 2019
Identification of flavonolignans from Silybum marianum seeds as allosteric protein tyrosine phosphatase 1B inhibitors.
Journal: Journal of enzyme inhibition and medicinal chemistry
Published: August 31, 2018
Design, synthesis, and biological evaluation of NAD(P)H: Quinone oxidoreductase (NQO1)-targeted oridonin prodrugs possessing indolequinone moiety for hypoxia-selective activation.
Journal: European journal of medicinal chemistry
Published: January 12, 2017
The conversion of oridonin to spirolactone-type or enmein-type diterpenoid: synthesis and biological evaluation of ent-6,7-seco-oridonin derivatives as novel potential anticancer agents.
Journal: European journal of medicinal chemistry
Published: January 14, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026