Works matching IS 18607179 AND DT 2018 AND VI 13 AND IP 5
Results: 9
Front Cover: Design and Synthesis of A‐Ring Simplified Pyripyropene A Analogues as Potent and Selective Synthetic SOAT2 Inhibitors (ChemMedChem 5/2018).
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- ChemMedChem, 2018, v. 13, n. 5, p. 399, doi. 10.1002/cmdc.201800104
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Hollow Mesoporous Silica@Metal–Organic Framework and Applications for pH‐Responsive Drug Delivery.
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- ChemMedChem, 2018, v. 13, n. 5, p. 400, doi. 10.1002/cmdc.201800019
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Comparative Pharmacological Study of Common NMDA Receptor Open Channel Blockers Regarding Their Affinity and Functional Activity toward GluN2A and GluN2B NMDA Receptors.
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- ChemMedChem, 2018, v. 13, n. 5, p. 446, doi. 10.1002/cmdc.201700810
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Development of Potent Inhibitors of the <italic>Mycobacterium tuberculosis</italic> Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside Macrophages.
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- ChemMedChem, 2018, v. 13, n. 5, p. 422, doi. 10.1002/cmdc.201700759
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Targeting the <italic>BCL2</italic> Gene Promoter G‐Quadruplex with a New Class of Furopyridazinone‐Based Molecules.
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- ChemMedChem, 2018, v. 13, n. 5, p. 406, doi. 10.1002/cmdc.201700749
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Simultaneous Multiple MS Binding Assays for the Dopamine, Norepinephrine, and Serotonin Transporters.
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- ChemMedChem, 2018, v. 13, n. 5, p. 453, doi. 10.1002/cmdc.201700737
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Discovery of Rogaratinib (BAY 1163877): a pan‐FGFR Inhibitor.
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- ChemMedChem, 2018, v. 13, n. 5, p. 437, doi. 10.1002/cmdc.201700718
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Design, Synthesis, and Biological Evaluation of Pyrazoline‐Based Hydroxamic Acid Derivatives as Aminopeptidase N (APN) Inhibitors.
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- ChemMedChem, 2018, v. 13, n. 5, p. 431, doi. 10.1002/cmdc.201700690
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- Article
Design and Synthesis of A‐Ring Simplified Pyripyropene A Analogues as Potent and Selective Synthetic SOAT2 Inhibitors.
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- ChemMedChem, 2018, v. 13, n. 5, p. 411, doi. 10.1002/cmdc.201700645
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- Article