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Inorganic Chemistry|October 11, 2005
Phosphate triester hydrolysis promoted by an N2S(thiolate)Zn complex: mechanistic implications for the metal-dependent reactivity of peptide deformylaseDavid P Goldberg, Robert C diTargiani, Frances Namuswe, et al.Biochemistry|January 20, 2017
Glutamate 350 Plays an Essential Role in Conformational Gating of Long-Range Radical Transport in Escherichia coli Class Ia Ribonucleotide ReductaseKanchana Ravichandran, Ellen C Minnihan, Qinghui Lin, et al.The AAPS Journal|November 16, 2014
Physicochemical and formulation developability assessment for therapeutic peptide delivery--a primerAnnette Bak, Dennis Leung, Stephanie E Barrett, et al.Proceedings of the National Academy of Sciences of the United States of America|February 23, 2013
Generation of a stable, aminotyrosyl radical-induced α2β2 complex of Escherichia coli class Ia ribonucleotide reductaseEllen C Minnihan, Nozomi Ando, Edward J Brignole, et al.Molecular Cancer Therapeutics|November 24, 2021
STimulator of INterferon Genes Agonism Accelerates Antitumor Activity in Poorly Immunogenic TumorsSamanthi A Perera, Johnny E Kopinja, Yanhong Ma, et al.RSC Medicinal Chemistry|August 6, 2021
Optimization of brain-penetrant picolinamide derived leucine-rich repeat kinase 2 (LRRK2) inhibitorsAnmol Gulati, Charles S Yeung, Blair Lapointe, et al.Science (New York, N.Y.)|August 22, 2020
An orally available non-nucleotide STING agonist with antitumor activityBo-Sheng Pan, Samanthi A Perera, Jennifer A Piesvaux, et al.ACS Medicinal Chemistry Letters|July 14, 2026
Discovery of MK-2118, a Small-Molecule Agonist of STINGTimothy Henderson, Michael D Altman, Alexei V Buevich, et al.Journal of Medicinal Chemistry|December 8, 2022
Discovery and Optimization of Potent, Selective, and Brain-Penetrant 1-Heteroaryl-1H-Indazole LRRK2 Kinase Inhibitors for the Treatment of Parkinson's DiseaseDavid A Candito, Vladimir Simov, Anmol Gulati, et al.Pageof 2