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Development of a whole‐cell high‐throughput phenotypic screen to identify inhibitors of mycobacterial amino acid biosynthesis.
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- FASEB Bioadvances, 2019, v. 1, n. 4, p. 246, doi. 10.1096/fba.2018-00048
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- Article
Novel inhibitors of Mycobacterium tuberculosis GuaB2 identified by a target based high-throughput phenotypic screen.
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- Scientific Reports, 2016, p. 38986, doi. 10.1038/srep38986
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- Article
Biochemical and Structural Characterization of Mycobacterial Aspartyl-tRNA Synthetase AspS, a Promising TB Drug Target.
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- PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0113568
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- Article
Tetrahydropyrazolo[1,5-<i>a</i>]Pyrimidine-3-Carboxamide and <i>N</i>-Benzyl-6′,7′-Dihydrospiro[Piperidine-4,4′-Thieno[3,2-<i>c</i>]Pyran] Analogues with Bactericidal Efficacy against <i>Mycobacterium tuberculosis</i> Targeting MmpL3.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060933
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- Article
Identification of Novel Imidazo[1,2-a]pyridine Inhibitors Targeting M. tuberculosis QcrB.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052951
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- Article
Direct Organocatalytic and Highly Enantio- and Diastereoselective Mannich Reactions of α-Substituted α-CyanoacetatesThis work was made possible by a grant from The Danish National Research Foundation. We are grateful to Dr. Jacob Overgaard for X-ray crystallographic analysis.
- Published in:
- Angewandte Chemie, 2005, v. 117, n. 19, p. 2956, doi. 10.1002/ange.200500144
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- Article
Direct Organocatalytic and Highly Enantio- and Diastereoselective Mannich Reactions of α-Substituted α-CyanoacetatesThis work was made possible by a grant from The Danish National Research Foundation. We are grateful to Dr. Jacob Overgaard for X-ray crystallographic analysis.
- Published in:
- Angewandte Chemie International Edition, 2005, v. 44, n. 19, p. 2896, doi. 10.1002/anie.200500144
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- Article