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Journal of Medicinal Chemistry|September 18, 2009
The replacement of His(4) in angiotensin IV by conformationally constrained residues provides highly potent and selective analoguesAneta Lukaszuk, Heidi Demaegdt, Debby Feytens, et al.
Journal of Medicinal Chemistry|September 18, 2009
Synthesis and antiprotozoal properties of pentamidine congeners bearing the benzofuran motifStanislav A Bakunov, Svetlana M Bakunova, Arlene S Bridges, et al.
Journal of Medicinal Chemistry|August 1, 1991
Synthesis of structural analogues of lyngbyatoxin A and their evaluation as activators of protein kinase CA P Kozikowski, P W Shum, A Basu, et al.
Journal of Medicinal Chemistry|August 1, 1991
Highly selective adenosine A2 receptor agonists in a series of N-alkylated 2-aminoadenosinesJ E Francis, R L Webb, G R Ghai, et al.
Journal of Medicinal Chemistry|August 30, 2008
Molecular engineering of conotoxins: the importance of loop size to alpha-conotoxin structure and functionAi-Hua Jin, Norelle L Daly, Simon T Nevin, et al.
Journal of Medicinal Chemistry|August 30, 2008
Lipid-lowering (hetero)aromatic tetrahydro-1,4-oxazine derivatives with antioxidant and squalene synthase inhibitory activityAngeliki P Kourounakis, Christos Charitos, Eleni A Rekka, et al.
Journal of Medicinal Chemistry|September 4, 2008
Design, synthesis, and biological evaluation of potent c-Met inhibitorsNoel D D'Angelo, Steven F Bellon, Shon K Booker, et al.
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