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Journal of Medicinal Chemistry|May 28, 2004
Sultam hydroxamates as novel matrix metalloproteinase inhibitorsRobert J Cherney, Ruowei Mo, Dayton T Meyer, et al.
Journal of Computer-Aided Molecular Design|December 26, 2016
Collaborating to improve the use of free-energy and other quantitative methods in drug discoveryBradley Sherborne, Veerabahu Shanmugasundaram, Alan C Cheng, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2007
Discovery of beta-benzamido hydroxamic acids as potent, selective, and orally bioavailable TACE inhibitorsJames J-W Duan, Lihua Chen, Zhonghui Lu, et al.
The Journal of Physical Chemistry. B|March 7, 2025
Prospective Evaluation of Structure-Based Simulations Reveal Their Ability to Predict the Impact of Kinase Mutations on Inhibitor BindingSukrit Singh, Vytautas Gapsys, Matteo Aldeghi, et al.
Toxicology and Applied Pharmacology|November 15, 2000
The species-dependent metabolism of efavirenz produces a nephrotoxic glutathione conjugate in ratsA E Mutlib, R J Gerson, P C Meunier, et al.
Biorxiv : the Preprint Server for Biology|March 10, 2025
Prospective evaluation of structure-based simulations reveal their ability to predict the impact of kinase mutations on inhibitor bindingSukrit Singh, Vytautas Gapsys, Matteo Aldeghi, et al.
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