Substituted ajoenes as novel anti-cancer agents

作者：Hunter Roger^*; Kaschula Catherine H; Parker Iqbal M; Caira Mino R; Richards Philip; Travis Susan; Taute Francois; Qwebani Thozama

来源：Bioorganic & Medicinal Chemistry Letters, 2008, 18(19): 5277-5279.

DOI：10.1016/j.bmcl.2008.08.056

• cancer
• garlic
• synthesis
• ajoene
• radical addition

A new synthesis of the ajoene pharmacophore core is presented involving the regioselective radical addition of a thiyl radical to a terminal alkyne as the key step. The synthesis allows structural variation of the two end groups on sulfur, and a range of novel derivatives varying the R(1) group (sulfoxide end) has been prepared and tested against CT-1 transformed. broblast cells for anti-cancer activity. The results indicate comparable or even improved activity compared to the parent natural product ajoene isomers. This opens up the way to systematically studying the biology of the ajoene core.

• 出版日期2008-10-1