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Chemmedchem|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 Heller
Chemmedchem|August 23, 2008
Targeting the open-flap conformation of HIV-1 protease with pyrrolidine-based inhibitorsJark Böttcher, Andreas Blum, Stefanie Dörr, et al.
Chemmedchem|August 23, 2008
Anti-inflammatory activity of a new class of nitric oxide synthase inhibitors that release nitric oxideMaurizio Botta, Eleonora Distrutti, Andrea Mencarelli, et al.
Chemmedchem|November 30, 2006
Macrocyclic aminopyrimidines as multitarget CDK and VEGF-R inhibitors with potent antiproliferative activitiesUlrich Lücking, Gerhard Siemeister, Martina Schäfer, et al.
Chemmedchem|January 26, 2007
Chemical tools to investigate sphingolipid metabolism and functionsAntonio Delgado, Josefina Casas, Amadeu Llebaria, et al.
Chemmedchem|April 5, 2007
Ensemble-docking approach on BACE-1: pharmacophore perception and guidelines for drug designVittorio Limongelli, Luciana Marinelli, Sandro Cosconati, et al.
Chemmedchem|December 28, 2006
Characterisation of the binding of cationic amphiphilic drugs to phospholipid bilayers using surface plasmon resonanceMatthew R Nussio, Matthew J Sykes, John O Miners, et al.
Chemmedchem|November 8, 2006
Arylthiopyrrole (AThP) derivatives as non-nucleoside HIV-1 reverse transcriptase inhibitors: synthesis, structure-activity relationships, and docking studies (part 1)Roberto Di Santo, Roberta Costi, Marino Artico, et al.
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