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Bioorganic & Medicinal Chemistry Letters|January 3, 2012
SAR studies of C2 ethers of 2H-pyrano[2,3-d]pyrimidine-2,4,7(1H,3H)-triones as nicotinic acid receptor (NAR) agonistXianhai Huang, Jing Su, Ashwin U Rao, et al.
Bioorganic & Medicinal Chemistry Letters|October 6, 2009
Tetrahydroquinoline sulfonamides as vasopressin 1b receptor antagonistsJack D Scott, Michael W Miller, Sarah W Li, et al.
Bioorganic & Medicinal Chemistry Letters|June 29, 2010
T-type calcium channel blockers: spiro-piperidine azetidines and azetidinones-optimization, design and synthesisElizabeth M Smith, Steve Sorota, Hyunjin M Kim, et al.
Bioorganic & Medicinal Chemistry Letters|March 7, 2012
Structure based design of iminohydantoin BACE1 inhibitors: identification of an orally available, centrally active BACE1 inhibitorJared N Cumming, Elizabeth M Smith, Lingyan Wang, et al.
Bioorganic & Medicinal Chemistry Letters|October 24, 2006
2,6-Disubstituted N-arylsulfonyl piperidines as gamma-secretase inhibitorsDmitri A Pissarnitski, Theodros Asberom, Thomas A Bara, et al.
ACS Medicinal Chemistry Letters|February 16, 2013
Discovery of an Orally Available, Brain Penetrant BACE1 Inhibitor that Affords Robust CNS Aβ ReductionAndrew W Stamford, Jack D Scott, Sarah W Li, et al.
Bioorganic & Medicinal Chemistry Letters|March 3, 2015
Iminopyrimidinones: a novel pharmacophore for the development of orally active renin inhibitorsBrian A McKittrick, John P Caldwell, Thomas Bara, et al.
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