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Bioorganic & Medicinal Chemistry Letters|August 6, 2002
Arylpiperazine substituted heterocycles as selective alpha(1a) adrenergic antagonistsHaripada Khatuya, Richard H Hutchings, Gee-Hong Kuo, et al.Bioorganic & Medicinal Chemistry Letters|November 8, 2006
Simplified staurosporine analogs as potent JAK3 inhibitorsShyh-Ming Yang, Ravi Malaviya, Lawrence J Wilson, 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|September 20, 2011
Discovery of novel Cobactin-T based matrix metalloproteinase inhibitors via a ring closing metathesis strategyLawrence J Wilson, Bingbing Wang, Shyh-Ming Yang, et al.ACS Medicinal Chemistry Letters|December 18, 2020
Discovery of PEGylated 6-Benzhydryl-4-amino-quinazolines as Peripherally Restricted CB<sub>1</sub>R Inverse AgonistsYue-Mei Zhang, Michael Greco, Tonya Le Blanc, et al.Bioorganic & Medicinal Chemistry Letters|May 26, 2007
Discovery of para-alkylthiophenoxyacetic acids as a novel series of potent and selective PPARdelta agonistsRui Zhang, Aihua Wang, Alan DeAngelis, 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.Bioorganic & Medicinal Chemistry Letters|March 14, 2017
Evaluation of anti-diabetic effect and gall bladder function with 2-thio-5-thiomethyl substituted imidazoles as TGR5 receptor agonistsXuqing Zhang, Zhihua Sui, Jack Kauffman, 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|December 19, 2007
beta-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: part 1. Design, synthesis, and lead identificationShyh-Ming Yang, Robert H Scannevin, Bingbing Wang, et al.Pageof 5