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Farmaco ; 53(1): 33-40, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9543724

ABSTRACT

Acyclic glycosidopyrroles of type 1, synthesized in good overall yields, were evaluated for anti-viral activity. Compound 10i was found to inhibit the HIV-1 replication at concentrations that were very close to those cytotoxic for MT-4 cells. Compounds 10a,f,i inhibited both strains HSV-1 and HSV-2 at concentrations slightly below those cytotoxic for Vero cells. However for this series of glycosidopyrroles some relationship between calculated log P values and the observed cytotoxicity was found.


Subject(s)
Antiviral Agents/chemical synthesis , Pyrroles/chemical synthesis , Animals , Antiviral Agents/pharmacology , Chlorocebus aethiops , Pyrroles/pharmacology , Vero Cells
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