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Published in 2019 at "Archiv der Pharmazie"
DOI: 10.1002/ardp.201800277
Abstract: A series of novel 3‐amidophenols with 5‐heteroatomic substitutions were designed and synthesized. Several compounds showed potent antitubercular activity against Mycobacterium tuberculosis H37Ra (MIC = 0.25–5 μg/mL). Compounds 12j and 14i also displayed good inhibitory activity against M. tuberculosis…
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Keywords:
design synthesis;
heteroatomic substitutions;
activity;
synthesis antitubercular ... See more keywords
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Published in 2017 at "Journal of Heterocyclic Chemistry"
DOI: 10.1002/jhet.2552
Abstract: Emergence of multidrug resistant and extensively drug resistant tuberculosis has prompted to develop new molecular entities to treat the disease. A series of new 4-thiazolidinones with pyrazinyl and thiazolyl scaffolds has been synthesized, and their…
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Keywords:
new thiazolidinones;
pyrazinyl thiazolyl;
thiazolyl scaffolds;
thiazolidinones pyrazinyl ... See more keywords
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Published in 2017 at "European journal of medicinal chemistry"
DOI: 10.1016/j.ejmech.2016.09.086
Abstract: A collection of 1,2,3-triazoles unsaturated fatty acid mimics were efficiently synthesized by click chemistry. The 1,4-disubstituted analogs prepared covered different alkyl chain lengths and triazole positions. The compounds were subsequently tested against Mycobacterium tuberculosis, being…
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Keywords:
fatty acid;
chemistry;
antitubercular activity;
activity triazolyl ... See more keywords
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Published in 2020 at "journal of applied pharmaceutical science"
DOI: 10.7324/japs.2021.110204
Abstract: Introduction: In a quest for developing active molecules to treat tuberculosis, we reported the design, synthesis, and antitubercular activity evaluation of benzo[1, 4]thiazin-3(4H)-one encompassed 1, 2, 4-triazoles targeting the DprE1 (Decaprenylphosphoryl-beta-D-ribose oxidase) enzyme involved in…
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Keywords:
evaluation;
design synthesis;
activity;
new benzothiazinone ... See more keywords