Found: 13
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Protein-protein interaction-based high throughput screening for adenylyl cyclase 1 inhibitors: Design, implementation, and discovery of a novel chemotype.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.977742
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- Article
Optimization of 2-Acylaminocycloalkylthiophene Derivatives for Activity against Staphylococcus aureus RnpA.
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- Antibiotics (2079-6382), 2021, v. 10, n. 4, p. 369, doi. 10.3390/antibiotics10040369
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- Article
Identification of Small Molecule Inhibitors of Staphylococcus aureus RnpA.
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- Antibiotics (2079-6382), 2019, v. 8, n. 2, p. 48, doi. 10.3390/antibiotics8020048
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- Article
Crystal structure of the ribonuclease‐P‐protein subunit from Staphylococcus aureus.
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- Acta Crystallographica: Section F, Structural Biology Communications, 2018, v. 74, n. 10, p. 632, doi. 10.1107/S2053230X18011512
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- Article
Optimization of 4‐Substituted Benzenesulfonamide Scaffold To Reverse Acinetobacter baumannii Serum‐Adaptive Efflux Associated Antibiotic Tolerance.
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- ChemMedChem, 2020, v. 15, n. 18, p. 1731, doi. 10.1002/cmdc.202000328
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- Article
Rational Development and Characterization of a Ubiquitin Variant with Selectivity for Ubiquitin C-Terminal Hydrolase L3.
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- Biomolecules (2218-273X), 2022, v. 12, n. 1, p. 62, doi. 10.3390/biom12010062
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- Article
Corrigendum: Ubiquitin C‐Terminal Hydrolase L1: Biochemical and Cellular Characterization of a Covalent Cyanopyrrolidine‐Based Inhibitor.
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- ChemBioChem, 2020, v. 21, n. 18, p. 2701, doi. 10.1002/cbic.202000493
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- Article
Ubiquitin C‐Terminal Hydrolase L1: Biochemical and Cellular Characterization of a Covalent Cyanopyrrolidine‐Based Inhibitor.
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- ChemBioChem, 2020, v. 21, n. 5, p. 712, doi. 10.1002/cbic.201900434
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- Article
Aryl Ethers from Arenediazonium Tetrafluoroborate Salts: from Neat Reactions to Solvent-mediated Effects.
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- Journal of the Iowa Academy of Science, 2009, v. 116, n. 1-4, p. 27
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- Article
In vitro and in vivo activities of the carbonic anhydrase inhibitor, dorzolamide, against vancomycin-resistant enterococci.
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- PeerJ, 2021, p. 1, doi. 10.7717/peerj.11059
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- Article
Optimization and Anti-Cancer Properties of Fluoromethylketones as Covalent Inhibitors for Ubiquitin C-Terminal Hydrolase L1.
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- Molecules, 2021, v. 26, n. 5, p. 1227, doi. 10.3390/molecules26051227
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- Article
Unguarded liabilities: Borrelia burgdorferi's complex amino acid dependence exposes unique avenues of inhibition.
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- Frontiers in Antibiotics, 2024, p. 1, doi. 10.3389/frabi.2024.1395425
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- Article
Optimization and Evaluation of Antiparasitic Benzamidobenzoic Acids as Inhibitors of Kinetoplastid Hexokinase 1.
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- ChemMedChem, 2017, v. 12, n. 23, p. 1994, doi. 10.1002/cmdc.201700592
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- Article