Suzuki Y J, Tsuchiya M, Safadi A, Kagan V E, Packer L
Department of Molecular & Cell Biology, University of California, Berkeley 94720.
Free Radic Biol Med. 1992 Nov;13(5):517-25. doi: 10.1016/0891-5849(92)90146-8.
Nitecapone [3-(3,4-dihydroxy-5-nitrophenyl)methylene-2,4-pentanedione] [OR-462] is a catechol-O-methyltransferase inhibitor with gastroprotective properties. Recently, its antioxidant properties have been discovered: It scavenges peroxyl radicals (ROO.) and thus spares glutathione. Further examination of the properties of nitecapone demonstrated a remarkable ability of this compound to act as an antioxidant: (1) to scavenge ROO. in solution with a stoichiometry factor of 2; (2) to scavenge ROO. in membranes; (3) to inhibit lipid peroxidation; (4) to act as a competitive inhibitor for xanthine oxidase with Ki of 8.8 microM; (5) to scavenge O2- with a second order kinetic rate constant of 1.0 x 10(4) M-1 s-1; and (6) to scavenge HO.. Nitecapone also interacts with oxidation product of ascorbate to participate in recycling of vitamin E. Thus, nitecapone potentially is an effective therapeutic antioxidant, and the use of this compound in a combination with other antioxidants may be beneficial.
硝替卡朋[3-(3,4-二羟基-5-硝基苯基)亚甲基-2,4-戊二酮][OR-462]是一种具有胃保护特性的儿茶酚-O-甲基转移酶抑制剂。最近,发现了其抗氧化特性:它能清除过氧自由基(ROO·),从而节省谷胱甘肽。对硝替卡朋特性的进一步研究表明,该化合物具有显著的抗氧化能力:(1)以化学计量系数2清除溶液中的ROO·;(2)清除膜中的ROO·;(3)抑制脂质过氧化;(4)作为黄嘌呤氧化酶的竞争性抑制剂,抑制常数Ki为8.8微摩尔;(5)以二阶动力学速率常数1.0×10⁴M⁻¹s⁻¹清除超氧阴离子(O₂⁻);(6)清除羟基自由基(HO·)。硝替卡朋还与抗坏血酸的氧化产物相互作用,参与维生素E的循环。因此,硝替卡朋可能是一种有效的治疗性抗氧化剂,将该化合物与其他抗氧化剂联合使用可能有益。