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Characterization of new, efficient Mycobacterium tuberculosis topoisomerase-I inhibitors and their interaction with human ABC multidrug transporters.
- Published in:
- PLoS ONE, 2018, v. 13, n. 9, p. 1, doi. 10.1371/journal.pone.0202749
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- Article
Update on the Discovery of Efflux Pump Inhibitors against Critical Priority Gram-Negative Bacteria.
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- Antibiotics (2079-6382), 2023, v. 12, n. 1, p. 180, doi. 10.3390/antibiotics12010180
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- Article
Regioselective and Stereoselective Synthesis of Parthenolide Analogs by Acyl Nitroso-Ene Reaction and Their Biological Evaluation against Mycobacterium tuberculosis.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 24, p. 17395, doi. 10.3390/ijms242417395
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- Article
Assessing the essentiality of the decaprenyl-phospho- d-arabinofuranose pathway in M ycobacterium tuberculosis using conditional mutants.
- Published in:
- Molecular Microbiology, 2014, v. 92, n. 1, p. 194, doi. 10.1111/mmi.12546
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- Article
Towards a new combination therapy for tuberculosis with next generation benzothiazinones.
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- EMBO Molecular Medicine, 2014, v. 6, n. 3, p. 372, doi. 10.1002/emmm.201303575
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- Article
A druggable secretory protein maturase of Toxoplasma essential for invasion and egress.
- Published in:
- eLife, 2017, p. 1, doi. 10.7554/eLife.27480
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- Article
Accelerated microfluidic native chemical ligation at difficult amino acids toward cyclic peptides.
- Published in:
- Nature Communications, 2018, v. 9, p. 1, doi. 10.1038/s41467-018-05264-8
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- Article
Towards a new tuberculosis drug: pyridomycin - nature's isoniazid.
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- EMBO Molecular Medicine, 2012, v. 4, n. 10, p. 1032, doi. 10.1002/emmm.201201689
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- Article
Pyridylpiperazine-based allosteric inhibitors of RND-type multidrug efflux pumps.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-021-27726-2
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- Article
Characterization of pyridylpiperazine-based efflux pump inhibitors for Acinetobacter baumannii.
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- JAC-Antimicrobial Resistance, 2023, v. 5, n. 5, p. 1, doi. 10.1093/jacamr/dlad112
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- Article
Pyridomycin bridges the NADH- and substrate-binding pockets of the enoyl reductase InhA.
- Published in:
- Nature Chemical Biology, 2014, v. 10, n. 2, p. 96, doi. 10.1038/nchembio.1405
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- Article