Title of article
Synthesis and cytotoxic activities of usnic acid derivatives Original Research Article
Author/Authors
Marc-Antoine Bazin، نويسنده , , Anne-Cécile Le Lamer، نويسنده , , Jean-Guy Delcros، نويسنده , , Isabelle Rouaud، نويسنده , , Philippe Uriac، نويسنده , , Joël Boustie، نويسنده , , Jean-Charles Corbel، نويسنده , , Sophie Tomasi، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
7
From page
6860
To page
6866
Abstract
Nine usnic acid–amine conjugates were evaluated on murine and human cancer cell lines. The polyamine derivatives showed significant cytotoxicity in L1210 cells. Their activities appeared to be independent of the polyamine transport system (PTS). Indeed, their activities were similar in chinese hamster ovary (CHO) and in the PTS deficient CHO-MG cells. In addition, α-difluoromethylornithine, an ornithine decarboxylase inhibitor known to indirectly enhance the activity of the PTS and consequently increase the cytotoxicity of cytotoxic drugs entering cells via the PTS, had no effect on the activity of the polyamine derivatives. The more active derivative (1,8-diaminooctane derivative) displayed similar activities on all cancer cell lines studied and induced apoptosis.
Keywords
Usnic acid–amine conjugation , apoptosis , Synthesis , Polyamine
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2008
Journal title
Bioorganic and Medicinal Chemistry
Record number
1306297
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