A9298

Methyl arachidonate

≥99% (GC)

• Sinónimos: Arachidonic acid methyl ester
• Fórmula empírica (notación de Hill): C₂₁H₃₄O₂
• Número de CAS: 2566-89-4
• Peso molecular: 318.49
• Beilstein: 1714445
• Número MDL: MFCD00016775
• Código UNSPSC: 12352211
• ID de la sustancia en PubChem: 24891434
• NACRES: NA.25

Propiedades

• origen biológico: Mortierella alpina
• Nivel de calidad: 200
• Ensayo: ≥99% (GC)
• Formulario: liquid
• grupo funcional: ester
• tipo de lípido: omega FAs
• Condiciones de envío: dry ice
• temp. de almacenamiento: −20°C
• cadena SMILES: CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC
• InChI: 1S/C21H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h7-8,10-11,13-14,16-17H,3-6,9,12,15,18-20H2,1-2H3/b8-7-,11-10-,14-13-,17-16-

Descripción

Aplicación

• Lipid peroxidation products mediate the formation of 8-hydroxydeoxyguanosine in DNA.: This article explores the role of lipid peroxidation products, specifically those involving methyl arachidonate, in causing oxidative DNA damage, indicating the compound′s influence on cellular aging and disease processes (Park JW et al., 1992).

Acciones bioquímicas o fisiológicas

Unlike most unsaturated fatty acid methyl esters, methyl arachidonate is a potent activator of protein kinase C at 5–50 μM. At the low end of the effective concentration range, the effect is due to cyclooxygenase products, while lipoxygenase products mediate the effect at higher concentrations.

Unlike most unsaturated fatty acid methyl esters, methyl arachidonate is a potent activator of protein kinase C.

Envase

Sealed ampule under vacuum.

Información de seguridad

• Código de clase de almacenamiento: 10 - Combustible liquids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)