Neoflavonoids as Inhibitors of HIV-1 Replication by Targeting the Tat and NF-κB Pathways

Twenty-eight neoflavonoids have been prepared and evaluated in vitro against HIV-1. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase reporter gene. Inhibition of HIV transcription and Tat function were tested on cells stably transfected with the HIV-LT...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2017-02, Vol.22 (2), p.321-321
Hauptverfasser: Olmedo, Dionisio A, López-Pérez, José Luis, Del Olmo, Esther, Bedoya, Luis M, Sancho, Rocío, Alcamí, José, Muñoz, Eduardo, Feliciano, Arturo San, Gupta, Mahabir P
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Sprache:eng
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Zusammenfassung:Twenty-eight neoflavonoids have been prepared and evaluated in vitro against HIV-1. Antiviral activity was assessed on MT-2 cells infected with viral clones carrying the luciferase reporter gene. Inhibition of HIV transcription and Tat function were tested on cells stably transfected with the HIV-LTR and Tat protein. Seven 4-phenylchromen-2-one derivatives showed HIV transcriptional inhibitory activity but only the phenylchrome-2-one inhibited NF-κB and displayed anti-Tat activity simultaneously. Compounds , , and , inhibited HIV replication in both targets at concentrations
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules22020321