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Bioorg Med Chem ; 11(7): 1577-82, 2003 Apr 03.
Article in English | MEDLINE | ID: mdl-12628681

ABSTRACT

HIV-1 integrase is a critical enzyme in the replication of HIV-1. It is absent in the host cells and therefore is a good target for treatment of HIV-1 infections. Integracides are members of the tetracyclic triterpenoids family that were isolated from the fermentation broth of a Fusarium sp. Integracide A, a sulfated ester, exhibited significant inhibitory activity against strand transfer reaction of HIV-1 integrase. The discovery, structure elucidation including single crystal X-ray structure and HIV-1 inhibitory activity of these compounds are described.


Subject(s)
Fusarium/metabolism , HIV Integrase Inhibitors/isolation & purification , HIV Integrase Inhibitors/pharmacology , HIV Integrase/drug effects , Triterpenes/chemical synthesis , Triterpenes/pharmacology , Crystallography, X-Ray , Fermentation , Humans , Magnetic Resonance Spectroscopy , Models, Molecular , Spectrometry, Mass, Electrospray Ionization
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