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Design, synthesis, and biological evaluation of m-amidophenol derivatives as a new class of antitubercular agents
A series of m-amidophenol derivatives (6a–6l, 7a–7q, 9a, 9b, 12a–12c, 14 and 15) were designed and synthesized. Their antitubercular activities were evaluated in vitro against M. tuberculosis strains H37Ra and H37Rv and clinically isolated multidrug-resistant M. tuberculosis strains. Ten compounds d...
Gorde:
| Argitaratua izan da: | Medchemcomm |
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| Egile Nagusiak: | , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Royal Society of Chemistry
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6096355/ https://ncbi.nlm.nih.gov/pubmed/30151083 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c8md00212f |
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