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Bioorg Med Chem Lett ; 19(7): 1977-81, 2009 Apr 01.
Article in English | MEDLINE | ID: mdl-19251416

ABSTRACT

The effects of introducing simple halogen, alkyl, and alkoxy substituents to the 4, 5, 6 and 7 positions of 1-(4-benzoylpiperazin-1-yl)-2-(1H-indol-3-yl)ethane-1,2-dione, an inhibitor of the interaction between HIV gp120 and host cell CD4 receptors, on activity in an HIV entry assay was examined. Small substituents at C-4 generally resulted in increased potency whilst substitution at C-7 was readily tolerated and uniformly produced more potent HIV entry inhibitors. Substituents deployed at C-6 and, particularly, C-5 generally produced a modest to marked weakening of potency compared to the prototype. Small alkyl substituents at N-1 exerted minimal effect on activity whilst increasing the size of the alkyl moiety led to progressively reduced inhibitory properties. These studies establish a basic understanding of the indole element of the HIV attachment inhibitor pharmacophore.


Subject(s)
HIV Fusion Inhibitors/chemistry , HIV Fusion Inhibitors/pharmacology , HIV-1/drug effects , Indoles/pharmacology , Virus Attachment/drug effects , Animals , Cell Line , Dogs , HIV Envelope Protein gp120/metabolism , HIV Infections/prevention & control , Humans , Indoles/chemistry , Indoles/pharmacokinetics , Rats , Structure-Activity Relationship
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