Home>>4-hydroxy Nonenal Glutathione-d3 (trifluoroacetate salt)

4-hydroxy Nonenal Glutathione-d3 (trifluoroacetate salt) Sale

(Synonyms: 4HNEGSHd3) 目录号 : GC46659

A neuropeptide with diverse biological activities

4-hydroxy Nonenal Glutathione-d3 (trifluoroacetate salt) Chemical Structure

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50 μg
¥1,713.00
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100 μg
¥3,255.00
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500 μg
¥13,705.00
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1 mg
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产品描述

4-hydroxy Nonenal Glutathione-d3 (4-HNE-GSH-d3 (trifluoroacetate salt) contains three deuterium atoms at the terminal methyl position. It is intended for use as an internal standard for the quantification of 4-HNE-GSH (trifluoroacetate salt) by GC- or LC-mass spectrometry. 4-hydroxy-Nonenal (4-HNE) is a major aldehyde produced during the lipid peroxidation of ω-6 polyunsaturated fatty acids, such as arachidonic acid and linoleic acid.1,2 4-HNE-GSH is a major adduct formed by the reaction of 4-HNE with GSH.3,4,5,6 4-HNE-GSH levels in liver, plasma, or isolated cells can serve as biomarkers for oxidative stress.7 The trapping of 4-HNE by glutathione to give HNE-GSH prevents the formation of DNA adducts with 4-HNE.8,9 In human polymorphonuclear leukocytes, HNE-GSH is metabolized to 1,4-dihydroxynonene glutathione (DHN-GSH), 4-hydroxynonenoic acid glutathione (HNA-GSH), and 4-hydroxy nonenal mercapturic acid (HNE-MA).3

1.Pryor, W.A., and Porter, N.A.Suggested mechanisms for the production of 4-hydroxy-2-nonenal from the autoxidation of polyunsaturated fatty acidsFree Radical Biology & Medicine8541-543(1990) 2.Esterbauer, H., Schaur, R.J., and Zoliner, H.Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde, and related aldehydesFree Radical Biology & Medicine1181-128(1991) 3.Siems, W., Crifo, C., Capuozzo, E., et al.Metabolism of 4-hydroxy-2-nonenal in human polymorphonuclear leukocytesArchives of Biochemistry and Biophysics503248-252(2010) 4.Laurent, A., Alary, J., Debrauwer, L., et al.Analysis in the rat of 4-hydroxynonenal metabolites excreted in bile: Evidence of enterohepatic circulation of these byproducts of lipid peroxidationChemical Research in Toxicology12887-894(1999) 5.Siems, W., and Grune, T.Intracellular metabolism of 4-hydroxynonenalMol.Aspects Med.24167-175(2003) 6.Alary, J., Fernandez, Y., Debrauwer, L., et al.Identification of intermediate pathways of 4-hydroxynonenal metabolism in the ratChemical Research in Toxicology16320-327(2003) 7.VÖlkel, W., Alvarez-SÁnchez, R., Weick, I., et al.Glutathione conjugates of 4-hydroxy-2(E)-nonenal as biomarkers of hepatic oxidative stress-induced lipid peroxidation in ratsFree Radical Biology & Medicine381526-1536(2005) 8.King, A.O., Corley, E.G., Anderson, R.K., et al.An efficient synthesis of LTD4 antagonist L-699,392The Journal of Organic Chemistry583731-3735(1993) 9.Falletti, O., Cadet, J., Favier, A., et al.Trapping of 4-hydroxynonenal by glutathione efficiently prevents formation of DNA adducts in human cellsFree Radical Biology & Medicine421258-1269(2007)

Chemical Properties

Cas No. N/A SDF
别名 4HNEGSHd3
Canonical SMILES O=C(NCC(O)=O)[C@H](CS[C@H]1CC(O)OC1CCCCC([2H])([2H])[2H])NC(CC[C@@H](N)C(O)=O)=O.FC(F)(C(O)=O)F
分子式 C19H30D3N3O8S.CF3COOH 分子量 580.6
溶解度 Water: 10 mg/ml 储存条件 Store at -20°C
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溶解性数据

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1 mM 1.7224 mL 8.6118 mL 17.2236 mL
5 mM 0.3445 mL 1.7224 mL 3.4447 mL
10 mM 0.1722 mL 0.8612 mL 1.7224 mL
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