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J Med Chem ; 27(7): 870-4, 1984 Jul.
Article in English | MEDLINE | ID: mdl-6737430

ABSTRACT

The in vivo antitumor activity and in vitro metabolic dealkylation have been measured for an homologous series of 3-alkyl-1-(4-carbamoylphenyl)-3-methyltriazenes and have been compared with their partition coefficients. This investigation has shown that the extent of oxidative metabolism in vitro and the antitumor activity in vivo of these compounds are dependent upon hydrophobicity. These findings provide confirmation for the relationship between metabolism and antitumor activity for aryldialkyltriazenes.


Subject(s)
Antineoplastic Agents/chemical synthesis , Triazenes/chemical synthesis , Animals , Chromatography, High Pressure Liquid , Female , Lymphoma/drug therapy , Mathematics , Mice , Mice, Inbred CBA , Microsomes, Liver/metabolism , Structure-Activity Relationship , Triazenes/therapeutic use
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