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Proceedings of the National Academy of Sciences of the United States of America|April 15, 2015
Inhibition of TLR2 signaling by small molecule inhibitors targeting a pocket within the TLR2 TIR domainPragnesh Mistry, Michelle H W Laird, Ryan S Schwarz, et al.
Chemistry & Biology|February 28, 2009
Structural basis for binding and selectivity of antimalarial and anticancer ethylenediamine inhibitors to protein farnesyltransferaseMichael A Hast, Steven Fletcher, Christopher G Cummings, et al.
Journal of Medicinal Chemistry|March 4, 2015
Perturbation of the c-Myc-Max protein-protein interaction via synthetic α-helix mimeticsKwan-Young Jung, Huabo Wang, Peter Teriete, et al.
Cancers|August 12, 2023
The Bivalent Bromodomain Inhibitor MT-1 Inhibits Prostate Cancer GrowthSanjeev Shukla, Carlos Riveros, Mohammed Al-Toubat, et al.
Plos One|October 25, 2016
Towards Development of Small Molecule Lipid II Inhibitors as Novel AntibioticsJamal Chauhan, Steven Cardinale, Lei Fang, et al.
Pulmonary Pharmacology & Therapeutics|August 23, 2021
CG223, a novel BET inhibitor, exerts TGF-β1-mediated antifibrotic effects in a murine model of bleomycin-induced pulmonary fibrosisShunya Kaneshita, Takashi Kida, Makoto Yoshioka, et al.
Journal of Medicinal Chemistry|September 15, 2006
Structurally simple, potent, Plasmodium selective farnesyltransferase inhibitors that arrest the growth of malaria parasitesMatthew P Glenn, Sung-Youn Chang, Carrie Hornéy, et al.
Theranostics|July 21, 2020
Nanotherapy delivery of c-myc inhibitor targets Protumor Macrophages and preserves Antitumor Macrophages in Breast CancerAlison K Esser, Michael H Ross, Francesca Fontana, et al.
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