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10.1371/journal.pone.0179100

http://scihub22266oqcxt.onion/10.1371/journal.pone.0179100
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C5489165!5489165!28658263
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suck abstract from ncbi


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pmid28658263      PLoS+One 2017 ; 12 (6): ä
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  • Identification of benzazole compounds that induce HIV-1 transcription #MMPMID28658263
  • Graci JD; Michaels D; Chen G; Schiralli Lester GM; Nodder S; Weetall M; Karp GM; Gu Z; Colacino JM; Henderson AJ
  • PLoS One 2017[]; 12 (6): ä PMID28658263show ga
  • Despite advances in antiretroviral therapy, HIV-1 infection remains incurable in patients and continues to present a significant public health burden worldwide. While a number of factors contribute to persistent HIV-1 infection in patients, the presence of a stable, long-lived reservoir of latent provirus represents a significant hurdle in realizing an effective cure. One potential strategy to eliminate HIV-1 reservoirs in patients is reactivation of latent provirus with latency reversing agents in combination with antiretroviral therapy, a strategy termed ?shock and kill?. This strategy has shown limited clinical effectiveness thus far, potentially due to limitations of the few therapeutics currently available. We have identified a novel class of benzazole compounds effective at inducing HIV-1 expression in several cellular models. These compounds do not act via histone deacetylase inhibition or T cell activation, and show specificity in activating HIV-1 in vitro. Initial exploration of structure-activity relationships and pharmaceutical properties indicates that these compounds represent a potential scaffold for development of more potent HIV-1 latency reversing agents.
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