Title of article
Elucidation of structure–activity relationships for 2- or 6-substituted-5,8-dimethoxy-1,4-naphthoquinones Original Research Article
Author/Authors
Rajeshwar P. Verma، نويسنده , , Corwin Hansch، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
13
From page
5997
To page
6009
Abstract
1,4-Naphthoquinones have already been recognized to possess a wide range of biological activities. We have developed quantitative structure activity relationships (QSAR) for different series of 2- or 6-substituted-5,8-dimethoxy-1,4-naphthoquinones to understand the chemical–biological interaction governing antiproliferative/cytotoxic activities against L1210 cells. QSAR results have shown that these activities of 2- or 6-substituted-5,8-dimethoxy-1,4-naphthoquinones depend largely on their hydrophobicity.
Keywords
CMR , MgVol , Hydrophobicity , QSAR , Naphthoquinone
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2004
Journal title
Bioorganic and Medicinal Chemistry
Record number
1303359
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