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ACS Medicinal Chemistry Letters|April 16, 2020
Strategic Incorporation of Polarity in Heme-Displacing Inhibitors of Indoleamine-2,3-dioxygenase-1 (IDO1)Catherine White, Meredeth A McGowan, Hua Zhou, et al.Journal of Medicinal Chemistry|January 28, 2015
Overcoming mutagenicity and ion channel activity: optimization of selective spleen tyrosine kinase inhibitorsJ Michael Ellis, Michael D Altman, Alan Bass, et al.Proceedings of the National Academy of Sciences of the United States of America|January 24, 2009
A class of selective antibacterials derived from a protein kinase inhibitor pharmacophoreJ Richard Miller, Steve Dunham, Igor Mochalkin, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2021
SAR towards indoline and 3-azaindoline classes of IDO1 inhibitorsWensheng Yu, Yongqi Deng, Brett Hopkins, et al.Journal of Medicinal Chemistry|March 3, 2022
Oxetane Promise Delivered: Discovery of Long-Acting IDO1 Inhibitors Suitable for Q3W Oral or Parenteral DosingDerun Li, David L Sloman, Abdelghani Achab, et al.ACS Medicinal Chemistry Letters|March 19, 2021
Carbamate and N-Pyrimidine Mitigate Amide Hydrolysis: Structure-Based Drug Design of Tetrahydroquinoline IDO1 InhibitorsDerun Li, Yongqi Deng, Abdelghani Achab, et al.Journal of Medicinal Chemistry|April 29, 2026
Discovery of Potent and Selective Benzothiophene Difluoromethyl Phosphonate (DFMP) PTPN2/N1-Dual InhibitorsXiao Mei Zheng, David A Candito, James Jewell, et al.Pageof 4