Abstract:
:Various anthraquinones substituted with hydroxyl, amino, halogen, carboxylic acid, substituted aromatic group, and sulfonate were tested to determine their activity against human immunodeficiency virus type 1 (HIV-1) in primary human lymphocytes. Among the compounds tested, polyphenolic and/or polysulfonate substituted anthraquinones were found to possess the most potent antiviral activity. Hypericin, an anthraquinone dimer previously shown to have activity against nonhuman retroviruses also exhibited anti-HIV-1 activity in lymphocytes. the active anthraquinones inhibited HIV-1 reverse transcriptase. However, this enzyme inhibition was selective only for 1,2,5,8-tetrahydroanthraquinone and hypericin. Hypericin interacts nonspecifically with protein suggesting that this effect may dictate its inhibitory activity against the viral reverse transcriptase.
journal_name
Antiviral Resjournal_title
Antiviral researchauthors
Schinazi RF,Chu CK,Babu JR,Oswald BJ,Saalmann V,Cannon DL,Eriksson BF,Nasr Mdoi
10.1016/0166-3542(90)90071-esubject
Has Abstractpub_date
1990-05-01 00:00:00pages
265-72issue
5eissn
0166-3542issn
1872-9096pii
0166-3542(90)90071-Ejournal_volume
13pub_type
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pub_type: 杂志文章
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journal_title:Antiviral research
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