Works matching IS 18607179 AND DT 2013 AND VI 8 AND IP 10
Results: 23
Spotlights on our sister journals: ChemMedChem 10/2013.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1584, doi. 10.1002/cmdc.201390043
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Interactions of the Multidrug Resistance Modulators Tariquidar and Elacridar and their Analogues with P-glycoprotein.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1701, doi. 10.1002/cmdc.201300233
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Drug Discovery: Practices, Processes, and Perspectives. Edited by Jie Jack Li and E. J. Corey.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1714, doi. 10.1002/cmdc.201300318
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Evaluating Prodrug Strategies for Esterase-Triggered Release of Alcohols.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1662, doi. 10.1002/cmdc.201300255
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A Conformational Mimetic Approach for the Synthesis of Carbocyclic Nucleosides as Anti-HCV Leads.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1673, doi. 10.1002/cmdc.201300277
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Synthesis, G-Quadruplex Stabilisation, Docking Studies, and Effect on Cancer Cells of Indolo[3,2- b]quinolines with One, Two, or Three Basic Side Chains.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1648, doi. 10.1002/cmdc.201300288
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Graphical Abstract: ChemMedChem 10/2013.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1575, doi. 10.1002/cmdc.201390042
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N-Substituted 1,2-Dihydroquinolines as Anticancer Agents: Electronic Control of Redox Stability, Assessment of Antiproliferative Effects, and Mechanistic Insights.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1623, doi. 10.1002/cmdc.201300210
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Blocking the Peroxisome Proliferator-Activated Receptor (PPAR): An Overview.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1609, doi. 10.1002/cmdc.201300250
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Metal-Based Compounds as Prospective Antileishmanial Agents: Inhibition of Trypanothione Reductase by Selected Gold Complexes.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1634, doi. 10.1002/cmdc.201300276
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Inside Cover: CONFECT: Conformations from an Expert Collection of Torsion Patterns (ChemMedChem 10/2013).
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- ChemMedChem, 2013, v. 8, n. 10, p. 1574, doi. 10.1002/cmdc.201390041
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In silico Optimization of a Fragment-Based Hit Yields Biologically Active, High-Efficiency Inhibitors for Glutamate Racemase.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1681, doi. 10.1002/cmdc.201390044
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CONFECT: Conformations from an Expert Collection of Torsion Patterns.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1690, doi. 10.1002/cmdc.201300242
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Disruption of Interactions between Hydrophobic Residues on Nonpolar Faces is a Key Determinant in Decreasing Hemolysis and Increasing Antimicrobial Activities of α-Helical Amphipathic Peptides.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1638, doi. 10.1002/cmdc.201390040
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Devalued and Distrusted: Can the Pharmaceutical Industry Restore its Broken Image?. By John L. LaMattina.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1715, doi. 10.1002/cmdc.201300279
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Cover Picture: Disruption of Interactions between Hydrophobic Residues on Nonpolar Faces is a Key Determinant in Decreasing Hemolysis and Increasing Antimicrobial Activities of α-Helical Amphipathic Peptides (ChemMedChem 10/2013).
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- ChemMedChem, 2013, v. 8, n. 10, p. 1573, doi. 10.1002/cmdc.201390040
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Targeting the K-Ras/PDE δ Protein-Protein Interaction: The Solution for Ras-Driven Cancers or Just Another Therapeutic Mirage?
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- ChemMedChem, 2013, v. 8, n. 10, p. 1620, doi. 10.1002/cmdc.201300311
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Back Cover: In silico Optimization of a Fragment-Based Hit Yields Biologically Active, High-Efficiency Inhibitors for Glutamate Racemase (ChemMedChem 10/2013).
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- ChemMedChem, 2013, v. 8, n. 10, p. 1720, doi. 10.1002/cmdc.201390044
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Tafamidis (Vyndaqel): A Light for FAP Patients.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1617, doi. 10.1002/cmdc.201300245
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Identification of the Binding Site of an Allosteric Ligand Using STD-NMR, Docking, and CORCEMA-ST Calculations.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1629, doi. 10.1002/cmdc.201300267
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Recent Advances in Inhibitors of Bacterial Fatty Acid Synthesis Type II (FASII) System Enzymes as Potential Antibacterial Agents.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1589, doi. 10.1002/cmdc.201300209
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Anti-HIV-1 Peptide Derivatives Based on the HIV-1 Co-receptor CXCR4.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1668, doi. 10.1002/cmdc.201300289
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Inhibition of Human α-Methylacyl CoA Racemase (AMACR): a Target for Prostate Cancer.
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- ChemMedChem, 2013, v. 8, n. 10, p. 1643, doi. 10.1002/cmdc.201300179
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