ARACHIDONIC ACID SODIUM SALT

ARACHIDONIC ACID SODIUM SALT Basic information
Product Name:ARACHIDONIC ACID SODIUM SALT
Synonyms:EICOSA-5Z,8Z,11Z,14Z-TETRAENOIC ACID;CIS,CIS,CIS,CIS-5,8,11, 14-EICOSATETRAENOIC ACID, NA;CIS,CIS,CIS,CIS-5,8,11,14-EICOSATETRAENOIC ACID SODIUM SALT;ARACHIDONIC ACID SODIUM SALT;ARACHIDONIC ACID, PORCINE LIVER, SODIUM SALT;5Z,8Z,11Z,14Z-EICOSATETRAENOIC ACID, SODIUM SALT;5,8,11,14-EICOSATETRAENOIC ACID;5,8,11,14-EICOSATETRAENOIC ACID SODIUM SALT
CAS:6610-25-9
MF:C20H31NaO2
MW:326.45
EINECS:
Product Categories:
Mol File:6610-25-9.mol
ARACHIDONIC ACID SODIUM SALT Structure
ARACHIDONIC ACID SODIUM SALT Chemical Properties
Fp 113℃
storage temp. -20°C
solubility methanol: 50 mg/mL, clear, colorless to faintly yellow
form waxy solid
color white to off-white
Safety Information
Risk Statements 19
WGK Germany 3
RTECS JX3874000
MSDS Information
ProviderLanguage
SigmaAldrich English
ARACHIDONIC ACID SODIUM SALT Usage And Synthesis
UsesArachidonic acid is used in assays to measure activity of oxidizing enzymes, such as cyclooxygenase, as well as in assays to determine platelet inhibition in whole blood. Arachidonic acid has been demonstrated to bind to the a subunit of G protein and inhibit the activity of Ras GTPase-activating proteins (GAPs), to have a role in the development and progression of prostate cancer, and to enhance formation of lipid bodies in human mast cells.
General DescriptionArachidonic acid (AA) is a polyunsaturated ? fatty acid constituent of the phospholipids of cell membranes. Structurally, it is a 20-carbon chain that contains four cis double bonds, which allow the free acid form of AA to be an insoluble oil; this can be converted to the water-soluble sodium salt form within the normal physiological pH range. Arachidonic acid is metabolized by multiple enzymes to yield various metabolites; AA and its metabolites play important roles in a variety of biological processes, including signal transduction, smooth muscle contraction, chemotaxis, cell proliferation and differentiation and apoptosis.
Biochem/physiol ActionsReleased arachidonic acid (AA) reacts with molecular oxygen nonenzymatically, through oxidative stress, and enzymatically through the action of oxygenase enzymes. AA is oxidized to prostaglandins and thromboxanes by at least two cyclooxygenase (COX) isoforms, to leukotrienes and lipoxins by lipoxygenases, and to epoxyeicosatrienoic acids via cytochrome p450-catalyzed metabolism. Cellular uptake of arachidonic acid is energy dependent and involves protein-facilitated transport across the plasma membrane.
ARACHIDONIC ACID SODIUM SALT Preparation Products And Raw materials
Taurine Calcium phosphate Linoleic acid FERROUS SULFATE CARRAGEENAN Phosphatidylserine Sucralose Magnesium chloride ARACHIDONIC ACID SODIUM SALT ARACHIDONYL ALCOHOL APPROX 99 Arachidonic acid

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