Works matching IS 18607179 AND DT 2012 AND VI 7 AND IP 6
Results: 25
Preview: ChemMedChem 7/2012.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1127, doi. 10.1002/cmdc.201290023
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Comparative Molecular Profiling of the PPARα/γ Activator Aleglitazar: PPAR Selectivity, Activity and Interaction with Cofactors.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1101, doi. 10.1002/cmdc.201100598
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Cover Picture: Hydroxamic Acids as Potent Inhibitors of Fe<sup>II</sup> and Mn<sup>II</sup> E. coli Methionine Aminopeptidase: Biological Activities and X-ray Structures of Oxazole Hydroxamate- EcMetAP-Mn Complexes (ChemMedChem 6/2012).
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- ChemMedChem, 2012, v. 7, n. 6, p. 937, doi. 10.1002/cmdc.201290024
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Back Cover: Discovery of 3 H-Imidazo[4,5- b]pyridines as Potent c-Met Kinase Inhibitors: Design, Synthesis, and Biological Evaluation (ChemMedChem 6/2012).
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- ChemMedChem, 2012, v. 7, n. 6, p. 1129, doi. 10.1002/cmdc.201290028
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Docetaxel Nanotechnology in Anticancer Therapy.
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- ChemMedChem, 2012, v. 7, n. 6, p. 952, doi. 10.1002/cmdc.201200052
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Elucidation of Mycobacterium tuberculosis Type II Dehydroquinase Inhibitors using a Fragment Elaboration Strategy.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1031, doi. 10.1002/cmdc.201100606
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Spotlights on our sister journals: ChemMedChem 6/2012.
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- ChemMedChem, 2012, v. 7, n. 6, p. 948, doi. 10.1002/cmdc.201290027
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Medicinal Chemistry of Nucleic Acids. Edited by Li He Zhang, Zhen Xi and Jyoti Chattopadhyaya.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1124, doi. 10.1002/cmdc.201200073
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Kinase Inhibitor Scaffolds against Neurodegenerative Diseases from a Southern Australian Ascidian, Didemnum sp.
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- ChemMedChem, 2012, v. 7, n. 6, p. 983, doi. 10.1002/cmdc.201200169
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Development of Selective Estrogen Receptor Modulator (SERM)-Like Activity Through an Indirect Mechanism of Estrogen Receptor Antagonism: Defining the Binding Mode of 7-Oxabicyclo[2.2.1]hept-5-ene Scaffold Core Ligands.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1094, doi. 10.1002/cmdc.201200048
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Synthesis, Anti-HIV Activity Studies, and in silico Rationalization of Cyclobutane-Fused Nucleosides.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1044, doi. 10.1002/cmdc.201200059
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Pentacycloundecane-diol-Based HIV-1 Protease Inhibitors: Biological Screening, 2 D NMR, and Molecular Simulation Studies.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1009, doi. 10.1002/cmdc.201100512
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Graphical Abstract: ChemMedChem 6/2012.
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- ChemMedChem, 2012, v. 7, n. 6, p. 939, doi. 10.1002/cmdc.201290026
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- Article
Discovery of 3 H-Imidazo[4,5- b]pyridines as Potent c-Met Kinase Inhibitors: Design, Synthesis, and Biological Evaluation.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1057, doi. 10.1002/cmdc.201200120
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Structure-Activity Relationships and Mechanism of Action of Eph-ephrin Antagonists: Interaction of Cholanic Acid with the EphA2 Receptor.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1071, doi. 10.1002/cmdc.201200102
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Exploration and Optimization of Structure-Activity Relationships in Drug Design using the Taguchi Method.
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- ChemMedChem, 2012, v. 7, n. 6, p. 977, doi. 10.1002/cmdc.201200106
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Therapeutic Oligonucleotides: Methods and Protocols. Edited by John Goodchild.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1125, doi. 10.1002/cmdc.201200072
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Synthesis of Gd and <sup>68</sup>Ga Complexes in Conjugation with a Conformationally Optimized RGD Sequence as Potential MRI and PET Tumor-Imaging Probes.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1084, doi. 10.1002/cmdc.201200043
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Hydroxamic Acids as Potent Inhibitors of Fe<sup>II</sup> and Mn<sup>II</sup> E. coli Methionine Aminopeptidase: Biological Activities and X-ray Structures of Oxazole Hydroxamate- EcMetAP-Mn Complexes.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1020, doi. 10.1002/cmdc.201200076
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- Article
Molecular Recognition of T:G Mismatched Base Pairs in DNA as Studied by Electrospray Ionization Mass Spectrometry.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1112, doi. 10.1002/cmdc.201100526
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Inside Cover: Pentacycloundecane-diol-Based HIV-1 Protease Inhibitors: Biological Screening, 2 D NMR, and Molecular Simulation Studies (ChemMedChem 6/2012).
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- ChemMedChem, 2012, v. 7, n. 6, p. 938, doi. 10.1002/cmdc.201290025
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Evaluation of Bis-Alkylamidoxime O-Alkylsulfonates as Orally Available Antimalarials.
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- ChemMedChem, 2012, v. 7, n. 6, p. 991, doi. 10.1002/cmdc.201200112
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Peptide Drug Discovery and Development: Translational Research in Academia and Industry. Edited by Miguel Castanho and Nuno C. Santos.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1123, doi. 10.1002/cmdc.201200178
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Synthesis, Structure Analysis, and Antitumor Evaluation of 3,6-Dimethyl-1,2,4,5-tetrazine-1,4-dicarboxamide Derivatives.
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- ChemMedChem, 2012, v. 7, n. 6, p. 973, doi. 10.1002/cmdc.201200109
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The Importance of the trans-Enamine Intermediate as a β-Lactamase Inhibition Strategy Probed in Inhibitor-Resistant SHV β-Lactamase Variants.
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- ChemMedChem, 2012, v. 7, n. 6, p. 1002, doi. 10.1002/cmdc.201200006
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