ARACHIDONIC ACID SODIUM SALT
Synonym(s):20:4, cis,cis,cis,cis-5,8,11,14-Eicosatetraenoic Acid, Na;5,8,11,14-Eicosatetraenoic acid;cis,cis,cis,cis-5,8,11,14-Eicosatetraenoic acid sodium salt, 20:4;Eicosa-5Z,8Z,11Z,14Z-tetraenoic acid;Sodium arachidonate
- CAS NO.:6610-25-9
- Empirical Formula: C20H31NaO2
- Molecular Weight: 326.45
- MDL number: MFCD00065458
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-04-23 13:52:06
What is ARACHIDONIC ACID SODIUM SALT?
The Uses of ARACHIDONIC ACID SODIUM SALT
Arachidonic 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.
What are the applications of Application
Arachidonic Acid Sodium Salt is a precursor for prostaglandins, prostacyclin, and thromboxane synthesis.
General Description
Arachidonic 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 Actions
Released 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.
Properties of ARACHIDONIC ACID SODIUM SALT
Flash point: | 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 for ARACHIDONIC ACID SODIUM SALT
Signal word | Warning |
Pictogram(s) |
Exclamation Mark Irritant GHS07 |
GHS Hazard Statements |
H315:Skin corrosion/irritation H319:Serious eye damage/eye irritation H335:Specific target organ toxicity, single exposure;Respiratory tract irritation |
Precautionary Statement Codes |
P261:Avoid breathing dust/fume/gas/mist/vapours/spray. P264:Wash hands thoroughly after handling. P264:Wash skin thouroughly after handling. P271:Use only outdoors or in a well-ventilated area. P280:Wear protective gloves/protective clothing/eye protection/face protection. P312:Call a POISON CENTER or doctor/physician if you feel unwell. P362:Take off contaminated clothing and wash before reuse. P302+P352:IF ON SKIN: wash with plenty of soap and water. P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. P403+P233:Store in a well-ventilated place. Keep container tightly closed. P501:Dispose of contents/container to..… |
Computed Descriptors for ARACHIDONIC ACID SODIUM SALT
New Products
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