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Design, synthesis, and biologic evaluation of novel galloyl derivatives as HIV-1 RNase H inhibitors
Human immunodeficiency virus (HIV) reverse transcriptase (RT)-associated ribonuclease H (RNase H) remains as the only enzyme encoded within the viral genome not targeted by current antiviral drugs. In this work, we report the design, synthesis, and biologic evaluation of a novel series of galloyl de...
Tallennettuna:
| Julkaisussa: | Chem Biol Drug Des |
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| Päätekijät: | , , , , , , , , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7441570/ https://ncbi.nlm.nih.gov/pubmed/30560566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cbdd.13455 |
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