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QSAR-driven Design, Synthesis and Discovery of Potent Chalcone Derivatives with Antitubercular Activity
New anti-tuberculosis (anti-TB) drugs are urgently needed to battle drug-resistant Mycobacterium tuberculosis strains and to shorten the current 6–12-month treatment regimen. In this work, we have continued the efforts to develop chalcone-based anti-TB compounds by using an in silico design and QSAR...
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| Pubblicato in: | Eur J Med Chem |
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| Autori principali: | , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6031314/ https://ncbi.nlm.nih.gov/pubmed/28582669 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ejmech.2017.05.026 |
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