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应用
6-羟基氯唑沙宗已用于基于 HPLC 的氯唑沙宗代谢分析 。
6-羟基氯唑沙宗已被用作：作为参考标准品，在重组人酶筛选中监测底物消耗或通过细胞色素 P450 家族 2 亚家族 E 成员 1 (CYP2E1) 所形成的 6-羟基氯唑沙宗。6-羟基氯唑沙宗已被用于基于高效液相色谱 (HPLC) 的氯唑沙宗代谢测定。
氯唑沙宗的 CYP2E1 & 1A2 代谢物。
生化/生理作用
6-羟基氯唑沙宗是一种新型氯唑沙宗代谢物。它是由细胞色素 P450 家族 2 亚家族 E 成员 1 (CYP2E1) 酶将氯唑沙宗羟基化形成的。确定 6-羟基氯唑沙宗的形成和清除被用作表征 CYP2E1 代谢活性的一种可靠标记。
包装
无底玻璃瓶。内含物装在插入的融合锥内。
制备说明
6-羟基氯唑沙宗可溶于甲醇。
警示用语：
Warning
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
In vitro CYP/FMO Reaction Phenotyping
Optimization in Drug Discovery: In Vitro Methods, 137-169 (2014)
C B Eap et al.
Journal of chromatography. B, Biomedical sciences and applications, 705(1), 139-144 (1998-03-14)
A gas chromatographic-mass spectrometric method is presented which allows the determination of chlorzoxazone and 6-hydroxychlorzoxazone after derivatization with the reagent N-tert.-butyldimethylsilyl-N-methyltrifluoroacetamide. No interference was observed from endogenous compounds following the extraction of plasma samples from six different human subjects. The
Drug Metabolism in Chronic Kidney Disease
Chronic Renal Disease, 1035-1051 (2020)
Eva González-Jasso et al.
Toxicology letters, 144(1), 55-67 (2003-08-16)
The inducibility of CYP2E1 was investigated in liver and peripheral lymphocytes of rats treated with benzene (0-10 mmol/kg body weight (bw), daily for 3 days, i.p., or 0 and 5 mmol/kg bw, daily for 14 days, i.p.) or toluene (0
Young Jin Moon et al.
Drug metabolism and disposition: the biological fate of chemicals, 31(6), 776-784 (2003-05-21)
The purpose of this study is to report the changes of CYP2E1, CYP1A2, CYP2B1/2, CYP2C11, CYP3A23, and CYP3A2 expression and pharmacokinetics and tissue distribution of chlorzoxazone (CZX) and 6-hydroxychlorzoxazone (OH-CZX) in rats with acute renal failure induced by uranyl nitrate
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