A9298

Methyl arachidonate

≥99% (GC)

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

Propriedades

• fonte biológica: Mortierella alpina
• Ensaio: ≥99% (GC)
• forma: liquid
• grupo funcional: ester
• tipo de lipídio: omega FAs
• Condições de expedição: dry ice
• temperatura de armazenamento: −20°C
• cadeia de caracteres 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-
• chave InChI: OFIDNKMQBYGNIW-ZKWNWVNESA-N

Descrição

Aplicação

• 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).

Ações bioquímicas/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.

Embalagem

Sealed ampule under vacuum.

Informações de segurança

• Código de classe de armazenamento: 10 - Combustible liquids
• Classe de risco de água (WGK): WGK 3
• Ponto de fulgor (°F): Not applicable
• Ponto de fulgor (°C): Not applicable
• Equipamento de proteção individual: Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)