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Journal of Medicinal Chemistry|June 19, 1998
Auxiliary agents for the peroral administration of peptide and protein drugs: synthesis and evaluation of novel pepstatin analoguesM Kratzel, R Hiessböck, A Bernkop-SchnürchJournal of Medicinal Chemistry|June 19, 1998
Nonsymmetric P2/P2' cyclic urea HIV protease inhibitors. Structure-activity relationship, bioavailability, and resistance profile of monoindazole-substituted P2 analoguesG V De Lucca, U T Kim, J Liang, et al.Journal of Medicinal Chemistry|June 19, 1998
Synthesis and dopamine transporter affinity of the four stereoisomers of (+/-)-2-(methoxycarbonyl)-7-methyl-3-phenyl-7-azabicyclo[2.2.1]heptaneC Zhang, S Izenwasser, J L Katz, et al.Journal of Medicinal Chemistry|May 23, 1998
Synthesis and biological activities of tricyclic conformationally restricted tetrahydropyrido annulated furo[2,3-d]pyrimidines as inhibitors of dihydrofolate reductasesA Gangjee, E Elzein, S F Queener, et al.Journal of Medicinal Chemistry|May 23, 1998
Development of a three-dimensional CysLT1 (LTD4) antagonist model with an incorporated amino acid residue from the receptorM E Zwaagstra, S H Schoenmakers, P H Nederkoorn, et al.Journal of Medicinal Chemistry|May 23, 1998
Clarification of the binding mode of teleocidin and benzolactams to the Cys2 domain of protein kinase Cdelta by synthesis of hydrophobically modified, teleocidin-mimicking benzolactams and computational docking simulationY Endo, S Takehana, M Ohno, et al.Journal of Medicinal Chemistry|May 23, 1998
Membrane-induced secondary structures of neuropeptides: a comparison of the solution conformations adopted by agonists and antagonists of the mammalian tachykinin NK1 receptorT L Whitehead, S D McNair, C E Hadden, et al.Journal of Medicinal Chemistry|May 23, 1998
Synthesis and biological activity of chimeric structures derived from the cytotoxic natural compounds dolastatin 10 and dolastatin 15J Poncet, M Busquet, F Roux, et al.Journal of Medicinal Chemistry|August 9, 2016
Development of a High-Affinity PET Radioligand for Imaging Cannabinoid Subtype 2 ReceptorRareş-Petru Moldovan, Rodrigo Teodoro, Yongjun Gao, et al.Journal of Medicinal Chemistry|August 12, 2016
Design and Synthesis of Pyridone-Containing 3,4-Dihydroisoquinoline-1(2H)-ones as a Novel Class of Enhancer of Zeste Homolog 2 (EZH2) InhibitorsPei-Pei Kung, Eugene Rui, Simon Bergqvist, et al.Pageof 3,134