Found: 23
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Dimethylthiazolidine Carboxylic Acid as a Rigid P3 Unit in Inhibitors of Serine Proteases: Application to Two Targets.
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- Chemical Biology & Drug Design, 2009, v. 74, n. 5, p. 517, doi. 10.1111/j.1747-0285.2009.00870.x
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- Article
Are the current commercially available oximes capable of reactivating acetylcholinesterase inhibited by the nerve agents of the A-series?
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- Archives of Toxicology, 2022, v. 96, n. 9, p. 2559, doi. 10.1007/s00204-022-03316-z
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- Article
Jumping from Fragment to Drug via Smart Scaffolds.
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- ChemMedChem, 2022, v. 17, n. 10, p. 1, doi. 10.1002/cmdc.202200092
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- Article
Development of LM98, a Small‐Molecule TEAD Inhibitor Derived from Flufenamic Acid.
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- ChemMedChem, 2021, v. 16, n. 19, p. 2982, doi. 10.1002/cmdc.202100432
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- Article
Front Cover: Fragment‐Based Phenotypic Lead Discovery: Cell‐Based Assay to Target Leishmaniasis (ChemMedChem 14/2018).
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- ChemMedChem, 2018, v. 13, n. 14, p. 1369, doi. 10.1002/cmdc.201800442
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- Article
Fragment‐Based Phenotypic Lead Discovery: Cell‐Based Assay to Target Leishmaniasis.
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- ChemMedChem, 2018, v. 13, n. 14, p. 1377, doi. 10.1002/cmdc.201800161
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- Article
Molecular modeling study of natural products as potential bioactive compounds against SARS-CoV-2.
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- Journal of Molecular Modeling, 2023, v. 29, n. 6, p. 1, doi. 10.1007/s00894-023-05586-5
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- Article
Modeling studies on the role of vitamins B1 (thiamin), B3 (nicotinamide), B6 (pyridoxamine), and caffeine as potential leads for the drug design against COVID-19.
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- Journal of Molecular Modeling, 2022, v. 28, n. 12, p. 1, doi. 10.1007/s00894-022-05356-9
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- Article
Reactivation of VX-Inhibited Human Acetylcholinesterase by Deprotonated Pralidoxime. A Complementary Quantum Mechanical Study.
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- Biomolecules (2218-273X), 2020, v. 10, n. 2, p. 192, doi. 10.3390/biom10020192
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- Article
The Conformation of a Peptidyl Methyl Ketone Inhibitor Bound to the Human Cytomegalovirus Protease.
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- Angewandte Chemie International Edition, 1998, v. 37, n. 19, p. 2729, doi. 10.1002/(SICI)1521-3773(19981016)37:19<2729::AID-ANIE2729>3.0.CO;2-4
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- Article
Ligand-Based Virtual Screening, Molecular Docking, Molecular Dynamics, and MM-PBSA Calculations towards the Identification of Potential Novel Ricin Inhibitors.
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- Toxins, 2020, v. 12, n. 12, p. 746, doi. 10.3390/toxins12120746
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- Article
Binding Mode Determination of Benzimidazole Inhibitors of the Hepatitis C Virus RNA Polymerase by a Structure and Dynamics StrategyWe are grateful to Dr. Michael Bös, Dr. Michael Cordingley, and Dr. Paul Anderson for encouragement and support. We also thank Dr. Timothy Stammers, Dr. Nathalie Goudreau, Dr. Marc-André Poupart, Dr. Dale Cameron, and Mr. Jeff O'Meara for comments or critical reading of the manuscript, as well as Ginette McKercher for determining inhibition constants.
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- Angewandte Chemie, 2004, v. 116, n. 33, p. 4406, doi. 10.1002/ange.200460326
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- Article
corrigendum: An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus.
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- 2003
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- Correction Notice
An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus.
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- Nature, 2003, v. 426, n. 6963, p. 186, doi. 10.1038/nature02099
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- Article
Binding Mode Determination of Benzimidazole Inhibitors of the Hepatitis C Virus RNA Polymerase by a Structure and Dynamics StrategyWe are grateful to Dr. Michael Bös, Dr. Michael Cordingley, and Dr. Paul Anderson for encouragement and support. We also thank Dr. Timothy Stammers, Dr. Nathalie Goudreau, Dr. Marc-André Poupart, Dr. Dale Cameron, and Mr. Jeff O'Meara for comments or critical reading of the manuscript, as well as Ginette McKercher for determining inhibition constants.
- Published in:
- Angewandte Chemie International Edition, 2004, v. 43, n. 33, p. 4306, doi. 10.1002/anie.200460326
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- Publication type:
- Article
Macrocyclic Inhibitors of the NS3 Protease as Potential Therapeutic Agents of Hepatitis C Virus Infection.
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- Angewandte Chemie International Edition, 2003, v. 42, n. 12, p. 1356, doi. 10.1002/anie.200390347
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- Publication type:
- Article
A Multi-epitope Vaccine Candidate Against Bolivian Hemorrhagic fever Caused by Machupo Virus.
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- Applied Biochemistry & Biotechnology, 2024, v. 196, n. 4, p. 2137, doi. 10.1007/s12010-023-04604-9
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- Article
Dynamic microfluidic single-cell screening identifies pheno-tuning compounds to potentiate tuberculosis therapy.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-48269-2
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- Article
Probing the free-state solution behavior of drugs and their tendencies to self-aggregate into nano-entities.
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- Nature Protocols, 2021, v. 16, n. 11, p. 5250, doi. 10.1038/s41596-021-00612-3
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- Article
Revealing Atropisomer Axial Chirality in Drug Discovery.
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- ChemMedChem, 2011, v. 6, n. 3, p. 505, doi. 10.1002/cmdc.201000485
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- Article
Cover Picture: Revealing Atropisomer Axial Chirality in Drug Discovery (ChemMedChem 3/2011).
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- ChemMedChem, 2011, v. 6, n. 3, p. 381, doi. 10.1002/cmdc.201190005
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- Article
The Use of Chemical Double-Mutant Cycles in Biomolecular Recognition Studies: Application to HCV NS3 Protease Inhibitors.
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- ChemMedChem, 2008, v. 3, n. 11, p. 1654, doi. 10.1002/cmdc.200800214
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- Article
The Challenge of Atropisomerism in Drug Discovery.
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- Angewandte Chemie International Edition, 2009, v. 48, n. 35, p. 6398, doi. 10.1002/anie.200901719
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- Article