Učitavanje...
The development of an effective synthetic route of rilpivirine
BACKGROUND: Rilpivirine (RPV) was approved by the U.S. FDA (Food and Drug Administration) in 2011 to treat individuals infected with human immunodeficiency virus 1 (HIV-1). Significantly, rilpivirine is three fold more potent than etravirine. Once-daily, it is used with a low oral dose (25 mg/tablet...
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| Izdano u: | BMC Chem |
|---|---|
| Glavni autori: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Springer International Publishing
2021
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8017658/ https://ncbi.nlm.nih.gov/pubmed/33810807 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13065-021-00749-y |
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