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Chemmedchem|December 17, 2008
How to extend the use of grid-based interaction energy maps from chemistry to biotopicsGiulia Caron, Alessandra Nurisso, Giuseppe ErmondiChemmedchem|December 19, 2008
Pyridylalanine-containing hydroxamic acids as selective HDAC6 inhibitorsStefan Schäfer, Laura Saunders, Sonja Schlimme, et al.Chemmedchem|December 19, 2008
Structural modifications of DAPY analogues with potent anti-HIV-1 activityXiao-Qing Feng, Yong-Hong Liang, Zhao-Sen Zeng, et al.Chemmedchem|December 23, 2008
(2,2-Diphenyl-[1,3]oxathiolan-5-ylmethyl)-(3-phenyl-propyl)-amine: a potent and selective 5-HT(1A) receptor agonistSilvia Franchini, Annalisa Tait, Adolfo Prandi, et al.Chemmedchem|May 7, 2009
Discovery of a potent, CNS-penetrant orexin receptor antagonist based on an n,n-disubstituted-1,4-diazepane scaffold that promotes sleep in ratsDavid B Whitman, Christopher D Cox, Michael J Breslin, et al.Chemmedchem|March 7, 2009
Synthesis and pharmacological activity of a potent inhibitor of the biosynthesis of the endocannabinoid 2-arachidonoylglycerolTiziana Bisogno, James J Burston, Ravi Rai, et al.Chemmedchem|May 29, 2009
Discovery of selective luteinizing hormone receptor agonists using the bivalent ligand methodKimberly M Bonger, Richard J B H N van den Berg, Annemiek D Knijnenburg, et al.Chemmedchem|June 9, 2009
Characterization of new PPARgamma agonists: benzimidazole derivatives - the importance of position 2Matthias Goebel, Bart Staels, Thomas Unger, et al.Chemmedchem|March 14, 2009
2-Phenylquinolones as inhibitors of the HIV-1 Tat-TAR interactionBarbara Gatto, Oriana Tabarrini, Serena Massari, et al.Chemmedchem|March 17, 2009
Structure-based optimization of benzoic acids as inhibitors of protein tyrosine phosphatase 1B and low molecular weight protein tyrosine phosphataseRosanna Maccari, Rosaria Ottanà, Rosella Ciurleo, et al.Pageof 462