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Correction: Juhás et al. Improving Antimicrobial Activity and Physico-Chemical Properties by Isosteric Replacement of 2-Aminothiazole with 2-Aminooxazole. Pharmaceuticals 2022, 15 , 580.
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- 2023
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- Correction Notice
Improving Antimicrobial Activity and Physico-Chemical Properties by Isosteric Replacement of 2-Aminothiazole with 2-Aminooxazole.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 5, p. 580, doi. 10.3390/ph15050580
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- Article
Synthesis, Biological Evaluation, and In Silico Modeling of N -Substituted Quinoxaline-2-Carboxamides.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 8, p. 768, doi. 10.3390/ph14080768
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- Article
N‐pyridinylbenzamides: an isosteric approach towards new antimycobacterial compounds.
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- Chemical Biology & Drug Design, 2021, v. 97, n. 3, p. 686, doi. 10.1111/cbdd.13804
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- Article
Synthesis and Antimicrobial Evaluation of 6-Alkylamino- N-phenylpyrazine-2-carboxamides.
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- Chemical Biology & Drug Design, 2015, v. 86, n. 4, p. 674, doi. 10.1111/cbdd.12536
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Towards Novel 3-Aminopyrazinamide-Based Prolyl-tRNA Synthetase Inhibitors: In Silico Modelling, Thermal Shift Assay and Structural Studies.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 15, p. 7793, doi. 10.3390/ijms22157793
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- Article
Adenosine-Mimicking Derivatives of 3-Aminopyrazine-2-Carboxamide: Towards Inhibitors of Prolyl-tRNA Synthetase with Antimycobacterial Activity.
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- Biomolecules (2218-273X), 2022, v. 12, n. 11, p. 1561, doi. 10.3390/biom12111561
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A hit expansion of 3‐benzamidopyrazine‐2‐carboxamide: Toward inhibitors of prolyl‐tRNA synthetase with antimycobacterial activity.
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- Archiv der Pharmazie, 2024, v. 357, n. 8, p. 1, doi. 10.1002/ardp.202400171
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- Article
Synthesis and anti-infective evaluation of 5-amino-N- -phenylpyrazine-2-carboxamides.
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- Czech & Slovak Pharmacy / Česká a Slovenská Farmacie, 2015, v. 64, n. 1/2, p. 19
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- Article
5-Alkylamino-N-phenylpyrazine-2-carboxamides: Design, Preparation, and Antimycobacterial Evaluation.
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- Molecules, 2020, v. 25, n. 7, p. 1561, doi. 10.3390/molecules25071561
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- Article
N-Pyrazinoyl Substituted Amino Acids as Potential Antimycobacterial Agents—the Synthesis and Biological Evaluation of Enantiomers.
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- Molecules, 2020, v. 25, n. 7, p. 1518, doi. 10.3390/molecules25071518
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- Article
Substituted N-(Pyrazin-2-yl)benzenesulfonamides; Synthesis, Anti-Infective Evaluation, Cytotoxicity, and In Silico Studies.
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- Molecules, 2020, v. 25, n. 1, p. 138, doi. 10.3390/molecules25010138
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- Article
Derivatives of 3-Aminopyrazine-2-carboxamides: Synthesis, Antimicrobial Evaluation, and in Vitro Cytotoxicity.
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- Molecules, 2019, v. 24, n. 7, p. 1212, doi. 10.3390/molecules24071212
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- Article
Design, Synthesis and Evaluation of N-pyrazinylbenzamides as Potential Antimycobacterial Agents.
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- Molecules, 2018, v. 23, n. 9, p. 2390, doi. 10.3390/molecules23092390
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The Forty-Sixth Euro Congress on Drug Synthesis and Analysis: Snapshot.
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- Molecules, 2017, v. 22, n. 11, p. 1848, doi. 10.3390/molecules22111848
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Ureidopyrazine Derivatives: Synthesis and Biological Evaluation as Anti-Infectives and Abiotic Elicitors.
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- Molecules, 2017, v. 22, n. 10, p. 1797, doi. 10.3390/molecules22101797
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- Article
Design, Synthesis, Antimycobacterial Evaluation, and In Silico Studies of 3-(Phenylcarbamoyl)-pyrazine-2-carboxylic Acids.
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- Molecules, 2017, v. 22, n. 9, p. 1491, doi. 10.3390/molecules22091491
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- Article
3-Substituted N-Benzylpyrazine-2-carboxamide Derivatives: Synthesis, Antimycobacterial and Antibacterial Evaluation.
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- Molecules, 2017, v. 22, n. 3, p. 495, doi. 10.3390/molecules22030495
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Synthesis of Novel Pyrazinamide Derivatives Based on 3-Chloropyrazine-2-carboxamide and Their Antimicrobial Evaluation.
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- Molecules, 2017, v. 22, n. 2, p. 223, doi. 10.3390/molecules22020223
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Synthesis and Biological Evaluation of N-Alkyl-3-(alkylamino)-pyrazine-2-carboxamides.
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- Molecules, 2015, v. 20, n. 5, p. 8687, doi. 10.3390/molecules20058687
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New Potentially Active Pyrazinamide Derivatives Synthesized Under Microwave Conditions.
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- Molecules, 2014, v. 19, n. 7, p. 9318, doi. 10.3390/molecules19079318
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Synthesis, Antimycobacterial Activity and In Vitro Cytotoxicity of 5-Chloro-N-phenylpyrazine-2-carboxamides.
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- Molecules, 2013, v. 18, n. 12, p. 14807, doi. 10.3390/molecules181214807
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Synthesis, Antimycobacterial, Antifungal and Photosynthesis-Inhibiting Activity of Chlorinated N-phenylpyrazine-2-carboxamides.
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- Molecules, 2010, v. 15, n. 12, p. 8567, doi. 10.3390/molecules15128567
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Substituted N-Phenylpyrazine-2-carboxamides: Synthesis and Antimycobacterial Evaluation.
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- Molecules, 2009, v. 14, n. 10, p. 4180, doi. 10.3390/molecules14104180
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Convergence conditions for a restarted GMRES method augmented with eigenspaces.
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- Numerical Linear Algebra with Applications, 2005, v. 12, n. 4, p. 373, doi. 10.1002/nla.421
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Generalization of convergence conditions for a restarted GMRES.
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- Numerical Linear Algebra with Applications, 2000, v. 7, n. 3, p. 117, doi. 10.1002/(SICI)1099-1506(200004/05)7:3<117::AID-NLA189>3.0.CO;2-Z
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