“氟西汀”、“氟伏沙明”、“酮康唑”、“奥美拉唑”、“舍曲林”、“噻氯匹定”、“反苯环丙胺”-"fluoxetine","fluvoxamine","ketoconazole","omeprazole","sertraline","ticlopidine","tranylcypromine"
注释ID
1184518588
变量_单倍型
CYP2C19*1, CYP2C19*19
基因
CYP2C19
药物名称(英)
"fluoxetine","fluvoxamine","ketoconazole","omeprazole","sertraline","ticlopidine","tranylcypromine"
药物名称(中)
“氟西汀”、“氟伏沙明”、“酮康唑”、“奥美拉唑”、“舍曲林”、“噻氯匹定”、“反苯环丙胺”
PMID
21692664
类型
Metabolism/PK
含义
yes
记事
The fluorogenic substrate 3-cyano-7-ethoxycoumarin (CEC) was incubated with CYP2C19 microsomal protein harboring human CYP2C19 variants to assay enzyme activity, standardized to protein concentration. "Sensitivity" refers to the extent of inhibition relative to CYP2C19*1A (WT) and quantified by IC50. The inhibitory effect of the following drugs was tested for each CYP2C19 variant: celecoxib, troglitazone, fluconazole, ketoconzale, omeprazole, ticlopidine, fluoxetine, sertraline, fluvoxamine, tranylcypromine.
专家论述
CYP2C19 *19 is associated with decreased sensitivity to fluoxetine, fluvoxamine, ketoconazole, omeprazole, sertraline, ticlopidine and tranylcypromine as compared to CYP2C19 *1.
等位基因
*19
专家评论
变体注释摘要
id研究类型特征类型
27072 Drug
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