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Bioorganic & Medicinal Chemistry Letters|June 26, 2003
Benzoxazinones as PPARgamma agonists. part 1: SAR of three aromatic regionsPhilip J Rybczynski, Roxanne E Zeck, Donald W Combs, et al.Bioorganic & Medicinal Chemistry Letters|September 24, 2004
Glycosylated dihydrochalcones as potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitorsJoseph Dudash, Xiaoyan Zhang, Roxanne E Zeck, et al.Bioorganic & Medicinal Chemistry Letters|November 1, 2003
2,5-disubstituted 3,4-dihydro-2H-benzo[b][1,4]thiazepines as potent and selective V2 arginine vasopressin receptor antagonistsMaud J Urbanski, Robert H Chen, Keith T Demarest, et al.Diabetes, Obesity & Metabolism|July 30, 2005
Pharmacological profile of a novel, non-TZD PPARgamma agonistX Chen, M C Osborne, P J Rybczynski, et al.Bioorganic & Medicinal Chemistry Letters|September 7, 2005
Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitorsJoseph Dudash, Yongzheng Zhang, John B Moore, et al.Journal of Medicinal Chemistry|December 30, 2003
Benzoxazinones as PPARgamma agonists. 2. SAR of the amide substituent and in vivo results in a type 2 diabetes modelPhilip J Rybczynski, Roxanne E Zeck, Joseph Dudash, et al.Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Synthesis and evaluation of nonpeptide substituted spirobenzazepines as potent vasopressin antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, et al.Bioorganic & Medicinal Chemistry Letters|December 29, 2005
Indole-glucosides as novel sodium glucose co-transporter 2 (SGLT2) inhibitors. Part 2Xiaoyan Zhang, Maud Urbanski, Mona Patel, et al.Bioorganic & Medicinal Chemistry Letters|October 4, 2005
Heteroaryl-O-glucosides as novel sodium glucose co-transporter 2 inhibitors. Part 1Xiaoyan Zhang, Maud Urbanski, Mona Patel, et al.Bioorganic & Medicinal Chemistry Letters|November 22, 2007
Design and synthesis of indane-ureido-thioisobutyric acids: A novel class of PPARalpha agonistsJay M Matthews, Xiaoli Chen, Ellen Cryan, et al.Pageof 3