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British Journal of Pharmacology|August 23, 2005
Sustained aquaretic effect of the V2-AVP receptor antagonist, RWJ-351647, in cirrhotic rats with ascites and water retentionJosefa Ros, Guillermo Fernández-Varo, Javier Muñoz-Luque, et al.Plos One|August 8, 2012
Beneficial metabolic effects of CB1R anti-sense oligonucleotide treatment in diet-induced obese AKR/J miceYuting Tang, George Ho, Yaxin Li, et al.Bioorganic & Medicinal Chemistry Letters|May 3, 2006
Synthesis and SAR of 1,3-disubstituted cyclohexylmethyl urea and amide derivatives as non-peptidic motilin receptor antagonistsSigmond G Johnson, Joseph W Gunnet, John B Moore, et al.Assay and Drug Development Technologies|August 3, 2004
Development of a sensitive and HTS-compatible reporter gene assay for functional analysis of human adenosine A2a receptors in CHO-K1 cellsYuting Tang, Jingqing Luo, Charles R Fleming, 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.Journal of Medicinal Chemistry|February 25, 2009
Design, synthesis, and biological evaluation of (2R,alphaS)-3,4-dihydro-2-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]-5-[3-(trifluoromethoxy)-phenyl]-alpha-(trifluoromethyl)-1(2H)-quinolineethanol as potent and orally active cholesteryl ester transfer protein inhibitorGee-Hong Kuo, Thomas Rano, Patricia Pelton, et al.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 7, 2005
Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitorsJoseph Dudash, Yongzheng Zhang, John B Moore, et al.Bioorganic & Medicinal Chemistry Letters|May 6, 2004
Synthesis and evaluation of spirobenzazepines as potent vasopressin receptor antagonistsMin Amy Xiang, Robert H Chen, Keith T Demarest, 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.Pageof 5