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Bioorganic & Medicinal Chemistry Letters|July 15, 2009
Potent aza-peptide derived inhibitors of HCV NS3 proteaseSrikanth Venkatraman, Wanli Wu, Neng-Yang Shih, et al.Organic Letters|December 4, 2004
Manipulation of N,O-nucleophilicity: efficient formation of 4-N-substituted 2,4-dihydro-3H-1,2,4-triazolin-3-onesXianhai Huang, Anandan Palani, Dong Xiao, et al.Accounts of Chemical Research|January 16, 2008
Challenges in modern drug discovery: a case study of boceprevir, an HCV protease inhibitor for the treatment of hepatitis C virus infectionF George Njoroge, Kevin X Chen, Neng-Yang Shih, et al.Organic Letters|July 5, 2007
Application of ring-closing metathesis for the synthesis of macrocyclic peptidomimetics as inhibitors of HCV NS3 proteaseFrancisco Velázquez, Srikanth Venkatraman, Wanli Wu, et al.Bioorganic & Medicinal Chemistry Letters|August 30, 2008
Benzimidazole-substituted (3-phenoxypropyl)amines as histamine H3 receptor ligandsRobert Aslanian, Xiaohong Zhu, Henry A Vaccaro, et al.Bioorganic & Medicinal Chemistry Letters|October 10, 2002
Synthesis and NK(1)/NK(2) binding activities of a series of diacyl-substituted 2-arylpiperazinesDavid J Blythin, Xiao Chen, John J Piwinski, et al.Organic Letters|February 14, 2006
Stereoselective synthesis of beta-substituted beta-amino sulfones and sulfonamides via addition of sulfonyl anions to chiral N-sulfinyl iminesFrancisco Velázquez, Ashok Arasappan, Kevin Chen, et al.Bioorganic & Medicinal Chemistry Letters|December 5, 2008
Discovery of novel spirocyclopropyl hydroxamate and carboxylate compounds as TACE inhibitorsZhuyan Guo, Peter Orth, Shing-Chun Wong, et al.Bioorganic & Medicinal Chemistry Letters|June 5, 2003
Identification of a dual histamine H1/H3 receptor ligand based on the H1 antagonist chlorpheniramineRobert Aslanian, Mwangi wa Mutahi, Neng-Yang Shih, et al.Bioorganic & Medicinal Chemistry Letters|August 6, 2002
Preparation of oxime dual NK(1)/NK(2) antagonists with reduced NK(3) affinityGregory A Reichard, Cheryl A Grice, Neng-Yang Shih, et al.Pageof 7