4-hydroxy Nonenal Mercapturic Acid
Product Specifications
CAS Number
146764-24-1
Target
Others|||Endogenous Metabolite
Related Pathways
Metabolism|||Others
Bioactivity
Peroxidation of common ?-6 polyunsaturated fatty acids (PUFAs) such as linoleic acid, DGLA, and arachidonic acid can give rise to 4-HNE. 4-HNE is cleared rapidly from the plasma and undergoes enterohepatic circulation as a glutathione conjugate in the rat. About two thirds of an administered dose of 4-HNE is excreted within 48 hours in the urine, primarily in the form of mercapturic acid conjugates. The C-1 aldehyde of 4-HNE is reduced to an alcohol in about half of these metabolites. The remainder are C-1 aldehydes or have been oxidized to C-1 carboxylic acids. These aldehydes and carboxylic acids can also form ?-lactols and ?-lactones, respectively, producing at least 4 or 5 end urinary metabolites of 4-HNE in vivo.
Smiles
CCCCCC1OC(O)CC1SC[C@H](NC(C)=O)C(O)=O
Molecular Formula
C14H25NO5S
Molecular Weight
319.42
Shipping Conditions
Cool pack
Storage Temperature
-20°C
Available Sizes
Curated Selection
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