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Thiamine disulfide as a potent inhibitor of human immunodeficiency virus (type-1) production.

Abstract：

:Thiol and disulfide compounds were tested as an anti-HIV drug against transactivator (Tat)-mediated transactivation of HIV-1. Of all the compounds tested, thiamine disulfide, alpha-lipoic acid, and N-acetycysteine significantly depressed HIV-1 Tat activity. Thiamine disulfide alone in these compounds possessing anti-HIV-Tat activity markedly inhibited production of progeny HIV-1 in acute and chronic HIV-1-infected CEM at nontoxic concentrations of 500-1000 microM. Thiamine disulfide (500 microM) blocked 99.7% of HIV-1 production after 96 hr culture in acute HIV-1 (LAV-1) infection (m.o.i. = 0.002), whereas it inhibited 90-98% of HIV-1 production in chronic-infected cells (CEM/LAV-1, H9/MN, and Molt-4/IIIB). The results suggest that thiamine disulfide may be important for AIDS chemotherapy.

journal_name

Biochem Biophys Res Commun

journal_title

Biochemical and biophysical research communications

authors

Shoji S,Furuishi K,Misumi S,Miyazaki T,Kino M,Yamataka K

doi

10.1006/bbrc.1994.2760

subject

Has Abstract

pub_date

1994-11-30 00:00:00

pages

967-75

issue

1

eissn

0006-291X

issn

1090-2104

pii

S0006-291X(84)72760-4

journal_volume

205

pub_type

杂志文章

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