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Idrugs : the Investigational Drugs Journal|December 15, 2010
Accelerating the discovery of new drug targets with chemical proteomicsAtwood K Cheung, Rishi K JainJournal of the American Chemical Society|September 26, 2002
Total syntheses of (+)- and (-)-cacospongionolide B: new insight into structural requirements for phospholipase A(2) inhibitionAtwood K Cheung, Marc L SnapperThe Journal of Organic Chemistry|August 17, 2004
Total syntheses of (+)- and (-)-cacospongionolide B, cacospongionolide e, and related analogues. Preliminary study of structural features required for phospholipase a2 inhibitionAtwood K Cheung, Ryan Murelli, Marc L SnapperAnnual Review of Pharmacology and Toxicology|August 9, 2011
Chemical genetics-based target identification in drug discoveryFeng Cong, Atwood K Cheung, Shih-Min A HuangThe Journal of Organic Chemistry|February 24, 2007
Conformationally restricted (+)-cacospongionolide B analogues. Influence on secretory phospholipase A2 inhibitionRyan P Murelli, Atwood K Cheung, Marc L SnapperJournal of Medicinal Chemistry|April 6, 2021
Use of Intramolecular 1,5-Sulfur-Oxygen and 1,5-Sulfur-Halogen Interactions in the Design of <i>N</i>-Methyl-5-aryl-<i>N</i>-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,4-thiadiazol-2-amine SMN2 Splicing ModulatorsJake Axford, Moo Je Sung, John Manchester, et al.Chemistry & Biology|July 30, 2013
PIKfyve, a class III PI kinase, is the target of the small molecular IL-12/IL-23 inhibitor apilimod and a player in Toll-like receptor signalingXinming Cai, Yongyao Xu, Atwood K Cheung, et al.Journal of Medicinal Chemistry|July 13, 2013
Identification of NVP-TNKS656: the use of structure-efficiency relationships to generate a highly potent, selective, and orally active tankyrase inhibitorMichael D Shultz, Atwood K Cheung, Christina A Kirby, et al.Journal of Medicinal Chemistry|November 9, 2018
Discovery of Small Molecule Splicing Modulators of Survival Motor Neuron-2 (SMN2) for the Treatment of Spinal Muscular Atrophy (SMA)Atwood K Cheung, Brian Hurley, Ryan Kerrigan, et al.Journal of Medicinal Chemistry|February 17, 2025
Discovery of GJG057, a Potent and Highly Selective Inhibitor of Leukotriene C4 SynthaseGebhard Thoma, Wolfgang Miltz, Rudolf Waelchli, et al.Pageof 2