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Mechanistic Studies and Modeling Reveal the Origin of Differential Inhibition of Gag Polymorphic Viruses by HIV-1 Maturation Inhibitors.
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- PLoS Pathogens, 2016, v. 12, n. 11, p. 1, doi. 10.1371/journal.ppat.1005990
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- Article
Severe acute respiratory syndrome coronavirus entry into host cells: Opportunities for therapeutic intervention.
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- Medicinal Research Reviews, 2006, v. 26, n. 4, p. 414, doi. 10.1002/med.20055
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- Article
Cover Feature: Intramolecular [2+2] Cycloaddition of N‐Allylcinnamamines and N‐Allylcinnamamides by Visible‐Light Photocatalysis (Eur. J. Org. Chem. 1/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 1, p. 3, doi. 10.1002/ejoc.201901849
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- Article
Intramolecular [2+2] Cycloaddition of N‐Allylcinnamamines and N‐Allylcinnamamides by Visible‐Light Photocatalysis.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 1, p. 41, doi. 10.1002/ejoc.201901482
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- Article
The alkylation of isatin-derived oximes: Spectroscopic and X-ray crystallographic structural characterization of oxime and nitrone products.
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- Journal of Heterocyclic Chemistry, 2009, v. 46, n. 3, p. 432, doi. 10.1002/jhet.84
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- Article
Chemical genetics strategy identifies an HCV NS5A inhibitor with a potent clinical effect.
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- Nature, 2010, v. 465, n. 7294, p. 96, doi. 10.1038/nature08960
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- Article
The crystal structure of NS5A domain 1 from genotype 1a reveals new clues to the mechanism of action for dimeric HCV inhibitors.
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- Protein Science: A Publication of the Protein Society, 2014, v. 23, n. 6, p. 723, doi. 10.1002/pro.2456
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- Article
Frontispiece: Tailor‐Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals.
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- Chemistry - A European Journal, 2020, v. 26, n. 50, p. 1, doi. 10.1002/chem.202085061
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- Article
Tailor‐Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals.
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- Chemistry - A European Journal, 2020, v. 26, n. 50, p. 11349, doi. 10.1002/chem.202000617
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- Article
Utilization of C(sp<sup>3</sup>)‐Carboxylic Acids and Their Redox‐Active Esters in Decarboxylative Carbon−Carbon Bond Formation.
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- Advanced Synthesis & Catalysis, 2021, v. 363, n. 15, p. 3693, doi. 10.1002/adsc.202100314
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- Article
Ligand‐Enabled β‐C(sp<sup>3</sup>)−H Lactamization of Tosyl‐Protected Aliphatic Amides Using a Practical Oxidant.
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- Angewandte Chemie International Edition, 2022, v. 61, n. 34, p. 1, doi. 10.1002/anie.202207354
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- Article
The discovery and evaluation of [<sup>18</sup>F]BMS-986229, a novel macrocyclic peptide PET radioligand for the measurement of PD-L1 expression and in-vivo PD-L1 target engagement.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2024, v. 51, n. 4, p. 978, doi. 10.1007/s00259-023-06527-3
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- Article
Antiviral activity and molecular mechanism of an orally active respiratory syncytial virus fusion inhibitor.
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- Journal of Antimicrobial Chemotherapy (JAC), 2005, v. 55, n. 3, p. 289, doi. 10.1093/jac/dkh558
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- Article
Resensitizing daclatasvir-resistant hepatitis C variants by allosteric modulation of NS5A.
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- Nature, 2015, v. 527, n. 7577, p. 245, doi. 10.1038/nature15711
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- Article
Inhibition of hERG Channel Trafficking: An Under-Explored Mechanism for Drug-Induced QT Prolongation.
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- ChemMedChem, 2009, v. 4, n. 2, p. 141, doi. 10.1002/cmdc.200990007
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- Article
Inhibition of hERG Channel Trafficking: An Under-Explored Mechanism for Drug-Induced QT Prolongation.
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- ChemMedChem, 2008, v. 3, n. 10, p. 1501, doi. 10.1002/cmdc.200800170
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- Article
Homology models of the HIV-1 attachment inhibitor BMS-626529 bound to gp120 suggest a unique mechanism of action.
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- Proteins, 2015, v. 83, n. 2, p. 331, doi. 10.1002/prot.24726
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- Article
Targeting acute ischemic stroke with a calcium-sensitive opener of maxi-K potassium channels.
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- Nature Medicine, 2001, v. 7, n. 4, p. 471, doi. 10.1038/86546
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- Article
Ligand‐Enabled β‐C(sp<sup>3</sup>)−H Lactamization of Tosyl‐Protected Aliphatic Amides Using a Practical Oxidant.
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- Angewandte Chemie, 2022, v. 134, n. 34, p. 1, doi. 10.1002/ange.202207354
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- Article
Development of a photoaffinity label for respiratory syncytial virus inhibitors.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2003, v. 46, n. 12, p. 1105
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- Article
Development of a photoaffinity label for respiratory syncytial virus inhibitors.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2003, v. 16, n. 12, p. 1105
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- Article
Stereoselective reduction via lithium borotritide: synthesis of <sup>3</sup>H-labeled 2-hydroxy-N-[(5-hydroxy-[5-<sup>3</sup>H]-1,3,3-trimethylcyclohexyl)methyl]-5-methylbenzamide.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1999, v. 42, n. 11, p. 1061, doi. 10.1002/(SICI)1099-1344(199911)42:11<1061::AID-JLCR261>3.0.CO;2-N
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- Article
Synthesis of <sup>3</sup>H-labeled 2-hydroxy-N-[(1,3,3-trimethyl-[4,5,6-<sup>3</sup>H]cyclohexyl)methyl]-5-azidobenzamide, a photoaffinity analog of an influenza fusion inhibitor.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1999, v. 42, n. 10, p. 965, doi. 10.1002/(SICI)1099-1344(199910)42:10<965::AID-JLCR255>3.0.CO;2-K
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- Article
Development, Characterization, and Radiation Dosimetry Studies of <sup>18</sup>F-BMS-986229, a <sup>18</sup>F-Labeled PD-L1 Macrocyclic Peptide PET Tracer.
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- Molecular Imaging & Biology, 2024, v. 26, n. 2, p. 301, doi. 10.1007/s11307-023-01889-4
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- Article