Works matching IS 18607179 AND DT 2018 AND VI 13 AND IP 8
Results: 13
Cover Feature: Insights into the Target Interaction of Naturally Occurring Muraymycin Nucleoside Antibiotics (ChemMedChem 8/2018).
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- ChemMedChem, 2018, v. 13, n. 8, p. 763, doi. 10.1002/cmdc.201800227
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Front Cover: Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants (ChemMedChem 8/2018).
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- ChemMedChem, 2018, v. 13, n. 8, p. 762, doi. 10.1002/cmdc.201800226
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A Sulfonozanamivir Analogue Has Potent Anti‐influenza Virus Activity.
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- ChemMedChem, 2018, v. 13, n. 8, p. 785, doi. 10.1002/cmdc.201800092
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Synthesis and Characterization of the R27S Genetic Variant of Insulin‐like Peptide 5.
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- ChemMedChem, 2018, v. 13, n. 8, p. 852, doi. 10.1002/cmdc.201800057
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Synthesis, Characterization, and Biodistribution of a Dinuclear Gadolinium Complex with Improved Properties as a Blood Pool MRI Agent.
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- ChemMedChem, 2018, v. 13, n. 8, p. 824, doi. 10.1002/cmdc.201800052
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5‐HT<sub>7</sub> Receptor Antagonists with an Unprecedented Selectivity Profile.
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- ChemMedChem, 2018, v. 13, n. 8, p. 795, doi. 10.1002/cmdc.201800026
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Natural Polyphenols Selectively Inhibit β‐Carbonic Anhydrase from the Dandruff‐Producing Fungus <italic>Malassezia globosa</italic>: Activity and Modeling Studies.
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- ChemMedChem, 2018, v. 13, n. 8, p. 816, doi. 10.1002/cmdc.201800015
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Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants.
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- ChemMedChem, 2018, v. 13, n. 8, p. 803, doi. 10.1002/cmdc.201700824
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Insights into the Target Interaction of Naturally Occurring Muraymycin Nucleoside Antibiotics.
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- ChemMedChem, 2018, v. 13, n. 8, p. 779, doi. 10.1002/cmdc.201700793
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Synthesis and Biological Evaluation of Imidazole‐Bearing α‐Phosphonocarboxylates as Inhibitors of Rab Geranylgeranyl Transferase (RGGT).
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- ChemMedChem, 2018, v. 13, n. 8, p. 842, doi. 10.1002/cmdc.201700791
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Application of Mono‐ and Disaccharides in Drug Targeting and Efficacy.
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- ChemMedChem, 2018, v. 13, n. 8, p. 764, doi. 10.1002/cmdc.201700762
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Design, Synthesis, and in vitro Evaluation of Multivalent Drug Linkers for High‐Drug‐Load Antibody–Drug Conjugates.
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- ChemMedChem, 2018, v. 13, n. 8, p. 790, doi. 10.1002/cmdc.201700722
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Stacking Interactions of Heterocyclic Drug Fragments with Protein Amide Backbones.
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- ChemMedChem, 2018, v. 13, n. 8, p. 835, doi. 10.1002/cmdc.201700721
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- Article