4-hydroxy Nonenal Glutathione (trifluoroacetate salt)

4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Suppliers list
Company Name: Shanghai Hongye Biotechnology Co. Ltd  
Tel: 400-9205774 400-920-5774
Email: sales@glpbio.cn
Company Name: ChemeGen(Shanghai) Biotechnology Co.,Ltd.  
Tel: 18818260767
Email: sales@chemegen.com
4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Basic information
Product Name:4-hydroxy Nonenal Glutathione (trifluoroacetate salt)
Synonyms:4-hydroxy Nonenal Glutathione (trifluoroacetate salt)
CAS:
MF:C31H49F3N6O16S2
MW:882.8765696
EINECS:
Product Categories:
Mol File:Mol File
4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Structure
4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Chemical Properties
solubility Water: 10 mg/ml
Safety Information
MSDS Information
4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Usage And Synthesis
Description4-hydroxy Nonenal Glutathione (HNE-GSH) is a major adduct formed by the reaction of 4-HNE with GSH.1,2,3,4 4-HNE-GSH levels in liver, plasma, or isolated cells can serve as biomarkers for oxidative stress.5 The trapping of 4-HNE by glutathione to give HNE-GSH prevents the formation of DNA adducts with 4-HNE.6,7 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).1WARNING This product is not for human or veterinary use.
References[1] WERNER SIEMS . Metabolism of 4-hydroxy-2-nonenal in human polymorphonuclear leukocytes[J]. Archives of biochemistry and biophysics, 2010, 503 2: Pages 248-252. DOI: 10.1016/j.abb.2010.08.018
[2] ALEXIA LAURENT. Analysis in the Rat of 4-Hydroxynonenal Metabolites Excreted in Bile: Evidence of Enterohepatic Circulation of These Byproducts of Lipid Peroxidation[J]. Chemical Research in Toxicology, 1999, 12 10: 887-894. DOI: 10.1021/tx9900425
[3] WERNER SIEMS  Tilman G. Intracellular metabolism of 4-hydroxynonenal[J]. Molecular Aspects of Medicine, 2003, 24 4: Pages 167-175. DOI: 10.1016/s0098-2997(03)00011-6
[4] JACQUES ALARY. Identification of Intermediate Pathways of 4-Hydroxynonenal Metabolism in the Rat[J]. Chemical Research in Toxicology, 2003, 16 3: 320-327. DOI: 10.1021/tx025671k
[5] WOLFGANG VÖLKEL . Glutathione conjugates of 4-hydroxy-2(E)-nonenal as biomarkers of hepatic oxidative stress-induced lipid peroxidation in rats[J]. Free Radical Biology and Medicine, 2005, 38 11: Pages 1526-1536. DOI: 10.1016/j.freeradbiomed.2005.02.015
[6] A. O. KING. An efficient synthesis of LTD4 antagonist L-699,392[J]. The Journal of Organic Chemistry, 1993, 58 14: 3731-3735. DOI: 10.1021/jo00066a027
[7] OLIVIER FALLETTI. Trapping of 4-hydroxynonenal by glutathione efficiently prevents formation of DNA adducts in human cells[J]. Free Radical Biology and Medicine, 2007, 42 8: Pages 1258-1269. DOI: 10.1016/j.freeradbiomed.2007.01.024
4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Preparation Products And Raw materials
Tag:4-hydroxy Nonenal Glutathione (trifluoroacetate salt) Related Product Information
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