Frank P, Novak R F
Biochem Biophys Res Commun. 1986 Nov 14;140(3):797-807. doi: 10.1016/0006-291x(86)90704-7.
The effects of three anthrapyrazoles and an aminoacridine derivative on doxorubicin- and iron-stimulated lipid peroxidation in rabbit hepatic microsomes have been characterized. Two anthrapyrazoles, CI-937 and CI-942, were potent inhibitors of lipid peroxidation with 15 microM drug inhibiting the rate of peroxidation 70 to 90%. In contrast CI-941 was relatively ineffective in inhibiting lipid peroxidation with only 35% inhibition occurring at 100 microM drug. CI-921, an aminoacridine derivative, diminished lipid peroxidation by 65% at 15 microM. All four drugs failed to decrease the rate of doxorubicin-stimulated NADPH oxidation at concentrations less than 50 microM, suggesting that inhibition of lipid peroxidation was not the result of diminished enzyme activity. CI-937 formed a 2:1 complex with ferric ion, KD = 47 microM, which was reversible with EDTA.
三种蒽吡唑类化合物和一种氨基吖啶衍生物对阿霉素和铁刺激的兔肝微粒体脂质过氧化的影响已得到表征。两种蒽吡唑类化合物CI-937和CI-942是脂质过氧化的有效抑制剂,15微摩尔药物可抑制70%至90%的过氧化速率。相比之下,CI-941在抑制脂质过氧化方面相对无效,在100微摩尔药物时仅发生35%的抑制。氨基吖啶衍生物CI-921在15微摩尔时可使脂质过氧化减少65%。在浓度低于50微摩尔时,所有四种药物均未能降低阿霉素刺激的NADPH氧化速率,这表明脂质过氧化的抑制不是酶活性降低的结果。CI-937与铁离子形成2:1复合物,解离常数KD = 47微摩尔,该复合物可被EDTA逆转。