Works matching IS 18607179 AND DT 2016 AND VI 11 AND IP 17
Results: 13
Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1904, doi. 10.1002/cmdc.201600180
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Synthesis and in vivo Evaluation of Fluorine-18 and Iodine-123 Pyrazolo[4,3- e]-1,2,4-triazolo[1,5- c]pyrimidine Derivatives as PET and SPECT Radiotracers for Mapping A<sub>2A</sub> Receptors.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1936, doi. 10.1002/cmdc.201600219
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Synthesis of Albicidin Derivatives: Assessing the Role of N-terminal Acylation on the Antibacterial Activity.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1899, doi. 10.1002/cmdc.201600231
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Fragment Screening of RORγt Using Cocktail Crystallography: Identification of Simultaneous Binding of Multiple Fragments.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1881, doi. 10.1002/cmdc.201600242
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Substrate Fragmentation for the Design of M. tuberculosis CYP121 Inhibitors.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1924, doi. 10.1002/cmdc.201600248
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16-Membered Macrolide Lactone Derivatives Bearing a Triazole-Functionalized Arm at the Aglycone C13 Position as Antibacterial and Anticancer Agents.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1886, doi. 10.1002/cmdc.201600250
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Dioxonaphthoimidazoliums are Potent and Selective Rogue Stem Cell Clearing Agents with SOX2-Suppressing Properties.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1944, doi. 10.1002/cmdc.201600262
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Fragment-Based Discovery of 5-Arylisatin-Based Inhibitors of Matrix Metalloproteinases 2 and 13.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1892, doi. 10.1002/cmdc.201600266
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Structure, Function, and Inhibition of Staphylococcus aureus Heptaprenyl Diphosphate Synthase.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1915, doi. 10.1002/cmdc.201600311
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BODIPY-Appended 2-(2-Pyridyl)benzimidazole Platinum(II) Catecholates for Mitochondria-Targeted Photocytotoxicity.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1956, doi. 10.1002/cmdc.201600320
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Cover Picture: Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches (ChemMedChem 17/2016).
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- ChemMedChem, 2016, v. 11, n. 17, p. 1876, doi. 10.1002/cmdc.201600429
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- Article
Back Cover: Structure, Function, and Inhibition of Staphylococcus aureus Heptaprenyl Diphosphate Synthase (ChemMedChem 17/2016).
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- ChemMedChem, 2016, v. 11, n. 17, p. 1968, doi. 10.1002/cmdc.201600430
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- Article
Spotlights on our sister journals: ChemMedChem 17/2016.
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- ChemMedChem, 2016, v. 11, n. 17, p. 1877, doi. 10.1002/cmdc.201681713
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- Article