Synthesis and anti-HIV activity of some non-nucleoside 2,3-disubstituted quinazoline derivatives (Part-V).
Indian J Exp Biol
;
1998 Dec; 36(12): 1280-3
Article
Dans Anglais
| IMSEAR
| ID: sea-59675
ABSTRACT
Several [2-phenyl-4(3H)-oxo-3-quinazolinylamino]-N-substituted- arylacetamides (1a-j) have been synthesized and tested at the National Cancer Institute, Bethesda, Maryland, USA, for their anti-HIV activity against susceptible human host cells (CEM cell line) over a wide range of concentrations (6.35 x 10(-8) to 2.00 x 10(-4) M). The highest protection observed is 45.67%. The structures of these compounds have been established on the basis of elemental analysis and spectral data.
Texte intégral:
Disponible
Indice:
IMSEAR (Asie du Sud-Est)
Sujet Principal:
Quinazolines
/
Humains
/
Tests de sensibilité microbienne
/
Lignée cellulaire
/
Agents antiVIH
langue:
Anglais
Texte intégral:
Indian J Exp Biol
Année:
1998
Type:
Article
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