Acetaminophen glucuronide

(Synonyms: APAP-glu)
目录号: PL02139 纯度: ≥99%
Acetaminophen glucuronide (APAP-glu) 是 Acetaminophen (HY-66005) 的无活性葡萄糖醛酸代谢物。Acetaminophen 是一种选择性环氧合酶 2 (COX-2) 抑制剂,也是有效的肝 N-乙酰转移酶 2 (NAT2) 抑制剂。
CAS No. :16110-10-4
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中文名称
Acetaminophen glucuronide
中文别名
(4-乙酰氨基苯基)-葡糖苷酸;对乙酰氨基酚-O-β-D-葡糖苷酸
英文名称
Acetaminophen glucuronide
英文别名
b-D-Glucopyranosiduronic acid,4-(acetylamino)phenyl;ACETAMINOPHEN GLUCURONIDE;Paracetamol β-D-glucuronide;[14C]-Acetaminophen glucuronide;4-glucuronosido-acetanilide;Acetaminophen D-glucuronide;acetaminophen O-beta-D-glucosiduronic acid;paracetamol glucuronide
Cas No.
16110-10-4
分子式
C14H17NO8
分子量
327.29
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
Acetaminophen glucuronide (APAP-glu) 是 Acetaminophen (HY-66005) 的无活性葡萄糖醛酸代谢物。Acetaminophen 是一种选择性环氧合酶 2 (COX-2) 抑制剂,也是有效的肝 N-乙酰转移酶 2 (NAT2) 抑制剂。
产品详情
Acetaminophen glucuronide (APAP-glu) 是 Acetaminophen (HY-66005) 的无活性葡萄糖醛酸代谢物。Acetaminophen 是一种选择性环氧合酶 2 (COX-2) 抑制剂,也是有效的肝 N-乙酰转移酶 2 (NAT2) 抑制剂。
生物活性
Acetaminophen glucuronide (APAP-glu) is an inactive glucuronide metabolite of Acetaminophen (HY-66005). Acetaminophen is a selective cyclooxygenase-2 (COX-2) inhibitor and a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor.
性状
Solid
IC50 & Target[1][2]
Human Endogenous Metabolite
体外研究(In Vitro)
Acetaminophen is metabolized in the liver mainly by glucuronidation and sulfation, thus generating the nontoxic metabolites, Acetaminophen glucuronide (APAP-glu). Acetaminophen glucuronide is a substrate for both canalicular Mrp2 and basolateral Mrp3 in rodents. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Carolina I Ghanem, et al. Shift from biliary to urinary elimination of acetaminophen-glucuronide in acetaminophen-pretreated rats. J Pharmacol Exp Ther. 2005 Dec;315(3):987-95.
[2]. Liudmila L Mazaleuskaya, et al. PharmGKB summary: pathways of acetaminophen metabolism at the therapeutic versus toxic doses. Pharmacogenet Genomics. 2015 Aug;25(8):416-26.
搜索质检报告(COA)
[1]. Carolina I Ghanem, et al. Shift from biliary to urinary elimination of acetaminophen-glucuronide in acetaminophen-pretreated rats. J Pharmacol Exp Ther. 2005 Dec;315(3):987-95.
[2]. Liudmila L Mazaleuskaya, et al. PharmGKB summary: pathways of acetaminophen metabolism at the therapeutic versus toxic doses. Pharmacogenet Genomics. 2015 Aug;25(8):416-26.

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2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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The dilution calculator equation
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