(±)5-iPF2α-VI-d11

目录号: GC46263纯度: >99.00%
An internal standard for the quantification of (±)5-iPF-VI

(±)5-iPF2α-VI-d11
Cas No.: 936565-17-2
规格价格库存数量操作
10 μg¥6,161.00现货
1
25 μg¥14,680.00现货
1

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产品描述 Description

(±)5-iPF-VI-d11 contains 11 deuterium atoms at the 16, 16, 17, 17, 18, 18, 19, 19, 20, 20, and 20 positions. It is intended for use as an internal standard for the quantification of (±)5-iPF-VI by GC- or LC-mass spectrometry. Isoprostanes are prostaglandin-like products of free-radical induced lipid peroxidation.1 Although the isoprostanes derived from arachidonic acid are the best characterized, many other polyunsaturated fatty acids can form isoprostanes.2 iPF-VI is one of dozens of possible stereo- and regioisomeric isoprostanes which can be formed from arachidonic acid. To date, the most extensively studied of these is 8-isoprostane (8-epi-PGF, iPF-III).3,4 However, 8-isoprostane is a minor isoprostane constituent when compared to some of the other isomers which form in natural conditions of oxidative stress,5 including iPF-VI of the type-VI isoprostanes. This class has been shown to be one of the major isoprostane products, in contrast to 8-isoprostane. In addition to being produced in greater abundance than 8-isoprostane, Type VI isoprostanes form internal lactones which facilitate their extraction and purification from biological samples.5,6,7,8

1.Morrow, J.D., Hill, K.E., Burk, R.F., et al.A series of prostaglandin F2-like compounds are produced in vivo in humans by a non-cyclooxygenase, free radical-catalyzed mechanismProc. Natl. Acad. Sci. U.S.A.87(23)9383-9387(1990) 2.Parchmann, S., and Mueller, M.J.Evidence for the formation of dinor isoprostanes E1 from α-linolenic acid in plantsThe Journal of Biological Chemisty27332650-32655(1998) 3.Delanty, N., Reilly, M., Pratico, D., et al.8-Epi PGF2α: Specific analysis of an isoeicosanoid as an index of oxidant stress in vivoBritish Journal of Clinical Pharmacology4215-19(1996) 4.Reilly, M.P., Barry, P., Lawson, J.A., et al.Urinary 8-epi PGF2α: An index of oxidant stress in vivoFibrinolysis & Proteolysis1181-84(1997) 5.Reilly, M.P., Pratico, D., Delanty, N., et al.Increased formation of distinct F2 isoprostanes in hypercholesterolemiaCirculation982822-2828(1998) 6.Li, H., Lawson, J.A., Reilly, M., et al.Quantitative high performance liquid chromatography/tandem mass spectrometric analysis of the four classes of F2-isoprostanes in human urineProceedings of the National Academy of Sciences of the United States of America96(23)13381-13386(1999) 7.Lawson, J.A., Li, H., Rokach, J., et al.Identification of two major F2 isoprostanes, 8,12-iso- and 5-epi-8,12-iso-isoprostane F2α-VI, in human urineThe Journal of Biological Chemisty27329295-29301(1998) 8.PraticÒ, D., Barry, O.P., Lawson, J.A., et al.IPF2α-I: An index of lipid peroxidation in humansProceedings of the National Academy of Sciences of the United States of America953449-3454(1998)

产品文档 Product Documents

Purity:>99.00%

化学性质Chemical Properties

CAS 号
936565-17-2
SMILES
CCCCC/C=C\C[C@H]1C(O)CC(O)[C@H]1\C=C\C(O)CCCC(=O)O
分子式
C20H23D11O5
分子量
365.6 g/mol
溶解性
DMF: 50 mg/ml,DMSO: 50 mg/ml,Ethanol: 50 mg/ml,PBS (pH 7.2): 1 mg/ml
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

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