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Chemmedchem|November 21, 2007
Sila-haloperidol, a silicon analogue of the dopamine (D2) receptor antagonist haloperidol: synthesis, pharmacological properties, and metabolic fateReinhold Tacke, Friedrich Popp, Barbara Müller, et al.Chemmedchem|June 26, 2008
Facile biocatalytic access to 9-fluorenylmethyl polyglycosides: evaluation of antiviral activity on immunocompetent cellsAnnabella Tramice, Adriana Arena, Ambra De Gregorio, et al.Chemmedchem|September 5, 2009
2-Acylaminopyridin-4-ylimidazoles as p38 MAP kinase inhibitors: Design, synthesis, and biological and metabolic evaluationsKatharina Ziegler, Dominik R J Hauser, Anke Unger, et al.Chemmedchem|August 29, 2009
Molecular fingerprint recombination: generating hybrid fingerprints for similarity searching from different fingerprint typesBritta Nisius, Jürgen BajorathChemmedchem|September 12, 2009
Studies on the synthesis and activity of three tripalladium complexes containing planaramine ligandsMohammad Farhad, Jun Qing Yu, Philip Beale, et al.Chemmedchem|September 15, 2009
From structure-activity to structure-selectivity relationships: quantitative assessment, selectivity cliffs, and key compoundsLisa Peltason, Ye Hu, Jürgen BajorathChemmedchem|November 29, 2008
C6-unsubstituted pyrazolo[3,4-d]pyrimidines are dual Src/Abl inhibitors effective against imatinib mesylate resistant chronic myeloid leukemia cell linesMaria Alessandra Santucci, Valentina Corradi, Manuela Mancini, et al.Chemmedchem|September 4, 2008
Computational studies to discover a new NR2B/NMDA receptor antagonist and evaluation of pharmacological profileRosaria Gitto, Laura De Luca, Stefania Ferro, et al.Chemmedchem|September 2, 2008
Apoptosis-inducing high (.)NO concentrations are not sustained either in nascent or in developed cancersAdam HellerChemmedchem|August 23, 2008
Targeting the open-flap conformation of HIV-1 protease with pyrrolidine-based inhibitorsJark Böttcher, Andreas Blum, Stefanie Dörr, et al.Pageof 461