Kuhnert Robert, Sárosi Menyhárt-Botond, George Sven, Lönnecke Peter, Hofmann Bettina, Steinhilber Dieter, Murganic Blagoje, Mijatovic Sanja, Maksimovic-Ivanic Danijela, Hey-Hawkins Evamarie
Institut für Anorganische Chemie, Universität Leipzig, Johannisallee 29, 04103, Leipzig, Germany.
Institut für Pharmazeutische Chemie, Johann-Wolfgang-Goethe-Universität Frankfurt, Max-von-Laue-Straße 9, 60438, Frankfurt, Germany.
ChemMedChem. 2017 Jul 6;12(13):1081-1086. doi: 10.1002/cmdc.201700309. Epub 2017 Jun 21.
The progression of cancer is accelerated by increased proliferation, angiogenesis, and inflammation. These processes are mediated by leukotrienes. Several cancer cell lines overexpress 5-lipoxygenase, an enzyme that converts arachidonic acid into leukotrienes. An early inhibitor of the 5-lipoxygenase pathway is Rev-5901, which, however, lacks in in vivo efficacy, as it is rapidly metabolized. We investigated the introduction of carboranes as highly hydrophobic and metabolically stable pharmacophores into lipoxygenase inhibitors. Carboranes are icosahedral boron clusters that are remarkably stable and used to increase the metabolic stability of unstable pharmaceutics without changing their biological activity. By introduction of meta-carborane into Rev-5901, the first carborane-based inhibitor of the 5-lipoxygenase pathway was obtained. We report the synthesis and inhibitory and cytotoxic behavior of these compounds toward several melanoma and colon cancer cell lines and their related anticancer mechanisms.
增殖、血管生成和炎症增加会加速癌症进展。这些过程由白三烯介导。几种癌细胞系过度表达5-脂氧合酶,该酶可将花生四烯酸转化为白三烯。5-脂氧合酶途径的早期抑制剂是Rev-5901,然而,它缺乏体内疗效,因为它会迅速代谢。我们研究了将具有高疏水性和代谢稳定性的药效基团碳硼烷引入脂氧合酶抑制剂。碳硼烷是二十面体硼簇,非常稳定,用于增加不稳定药物的代谢稳定性而不改变其生物活性。通过将间碳硼烷引入Rev-5901,获得了首个基于碳硼烷的5-脂氧合酶途径抑制剂。我们报道了这些化合物对几种黑色素瘤和结肠癌细胞系的合成、抑制和细胞毒性行为及其相关的抗癌机制。