Department of Chemistry, University of British Columbia, 2036, Main Mall, Vancouver, British Columbia, V6T 1Z1, Canada.
Curr Top Med Chem. 2014;14(7):865-74. doi: 10.2174/1568026614666140202204602.
Mechanism-based inhibitors are relatively chemically inert compounds that become activated when processed by their target enzyme, leading to covalent enzyme inactivation. Fluorine substitution confers a number of properties that are beneficial to the chemistry of such inhibitors and to their potential use as pharmaceuticals, and indeed several fluorinated mechanism-based inhibitors have made it to clinical usage over the past 50 years. Well-known examples are the 5- fluorouracil metabolite, 5-fluoro-2'-deoxyuridine-5'-monophosphate, which is used in the treatment of cancer, and α- difluoromethylornithine for the treatment of African sleeping sickness. As the prevalence of fluorine in medicinal chemistry continues to rise, more and more medically relevant fluorinated mechanism-based inhibitors are being developed with a variety of interesting properties and uses.
基于机制的抑制剂是相对化学惰性的化合物,当被其靶酶处理时会被激活,导致共价酶失活。氟取代赋予了许多有益于此类抑制剂化学性质的特性,以及它们作为药物的潜在用途,事实上,在过去的 50 年中,已经有几种氟化的基于机制的抑制剂被应用于临床。著名的例子是 5-氟尿嘧啶代谢物 5-氟-2'-脱氧尿苷-5'-单磷酸,它被用于癌症的治疗,以及α-二氟甲基鸟氨酸用于治疗非洲昏睡病。随着氟在药物化学中的应用不断增加,越来越多具有各种有趣性质和用途的具有医学相关性的氟化基于机制的抑制剂正在被开发。