Il Farmaco

2, 1, 3-Benzothiadiazine derivatives: synthesis and screening versus PDE4 enzyme

A Tait, A Luppi, R Avallone, M Baraldi

文献索引：Tait, Annalisa; Luppi, Amedeo; Avallone, Rossella; Baraldi, Mario Farmaco, 2005 , vol. 60, # 8 p. 653 - 663

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被引用次数: 1

摘要

A series of N-1, 3 disubstituted 2, 1, 3-benzothiadiazine derivatives (BTDs) were synthesized and evaluated for their inhibitory activity versus enzymatic isoform PDE4 extracted from U937 cell line. Some of the tested compounds showed a high PDE4 inhibitory activity at 100 μM and the IC50 value of the most interesting terms were evaluated. The structure–activity relationships of these compounds showed that the 3, 5-di-tert-butyl-4-hydroxybenzyl ...