参考文献:
[1]黄春连,范雪梅,黎倩,等.制何首乌对大鼠肝脏P450酶5种亚型mRNA表达的影响[J].中国中药杂志,2017,42(2):352-356.
[2]杨晓霞,张薇,龚久平,等.蚯蚓细胞色素P450酶系对土壤中芘或苯并[a]芘的响应[J].环境科学学报,2017,37(10):4019-4025.
[3]徐鹿,赵春青,徐德进,等.亚致死剂量氟啶虫胺腈对灰飞虱细胞色素P450的影响[J].植物保护学报,2017,44(4):679-686.
[4]刘萍,边强.细胞色素P450酶系对药物生化转化的作用[J].国外医药(合成药 生化药制剂分册),2000,21(5):305-306.
[5]Dydio P,Key H M,Hayashi H,et al.Chemoselective, enzymatic C-H bond amination catalyzed by a cytochrome P450 containing an Ir (Me)-PIX cofactor[J].Journal of the American Chemical Society,2017,139(5):1750-1753.
[6]Manikandan P,Nagini S.Cytochrome P450 Structure, Function and Clinical Significance: A Review[J].Current Drug Targets,2018,19(1):38-54.
[7]Cuyue T,Magang S,David R.Substrate dependent effect of acetonitrilein human liver microsomal cytochrome P450 2C9 activity[J].Drug metab Dipos,2000,28(5):567-572.
[8]陈毓荃.生物化学试验方法和技术[M].北京:科学出版社,2002:96-97.
[9]Omura T,Sato R.The carbon monoxide-binding pigment of liver mocrosomes[J].Biol chem,1964,239(7):2370-2378.
[10]Nelson C H,Kirby B J,Lu N,et al.Evaluation of cytochrome P450-and transporter-mediated drug-drug interactions with the farnesoid x receptor agonist GS9674 and phenotypic probe substrates and inhibitors/inducers[J].Journal of Hepatology,2017,66(1):S151.
[11]唐跃年,张顺国,李岚,等.肝细胞微粒体的制备和细胞素P450氧化酶活性测定[J].中国医院药学杂志,1998,18(12):535-536.
[12]Baker S C,Arlt V M,Indra R,et al.Cytochrome P450 activity in muscle-invasive bladder cancer: A novel sub-group[J]//Urologic Oncology,2017,35(10):608.
[13]黄春连,范雪梅,黎倩,等.制何首乌对大鼠肝脏P450酶5种亚型mRNA表达的影响[J].中国中药杂志,2017,42(2):352-356.
[14]Huang Q,Deshmukh R S,Ericksen S S,et al.Preferred binding orientations of phenacetin in CYP1A1 and CYP1A2 are associated with isoform-selective metabolism[J].Drug Metabolism and Disposition,2012,40(12):2324-2331.
[15]陈大健.鲫鱼肝微粒体细胞色素P450酶系的初步研究[D].南京:南京农业大学,2006.
[16]杨海峰.鸡肝微粒体的细胞色素P450酶系的初步研究[D].南京:南京农业大学,2006.
[17]李在建,吴玉荣,易维学,等.3种不同磺胺类药物对鲤鱼肝细胞色素P450酶系生化指标的影响[J].中国兽医科学,2010,40(9):970-974.
[18]殷亦情,张博.四环素类抗生素研究进展情况[J].南方农机,2018,49(3):190,193. |