2692624-39-6
Chemical Structure
Methyl arachidonate-13C4
Synonym(s): Arachidonic acid methyl ester-13C4
- CAS No.: 2692624-39-6
- Formula:C1713C4H34O2
- Molecular Weight:322.46
IUPAC Name: methyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate-2,3,4,5-13C4
InChIKey: OFIDNKMQBYGNIW-HNOVROEYSA-N
SMILES: CCCCC/C=C\C/C=C\C/C=C\C/C=[13CH]\[13CH2][13CH2][13CH2]C(OC)=O
Biological Activity: Methyl arachidonate-13C4 (Arachidonic acid methyl ester-13C4) is 13C labeled Methyl arachidonate. Methyl arachidonate (Arachidonic acid methyl ester) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol. Methyl arachidonate has activity of human blood serum metabolite[1][1][2].
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Methyl arachidonate-13C4 | Methyl arachidonate-13C4 (Arachidonic acid methyl ester-13C4) is 13C labeled Methyl arachidonate. Methyl arachidonate (Arachidonic acid methyl ester) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol. Methyl arachidonate has activity of human blood serum metabolite. | |||||||||||||||||||||
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Methyl arachidonate-d5 | Methyl arachidonate-d5 is the deuterium labeled Arachidonic acid methyl ester. | |||||||||||||||||||||
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Methyl arachidonate-d8 | 99.9% | Methyl arachidonate-d8 is the deuterium labeled Arachidonic acid methyl ester. | ||||||||||||||||||||
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Methyl arachidonate-13C5 | Methyl arachidonate-13C5 (Arachidonic acid methyl ester-13C5) is 13C labeled Methyl arachidonate. Methyl arachidonate (Arachidonic acid methyl ester) is a fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol. Methyl arachidonate has activity of human blood serum metabolite. | |||||||||||||||||||||
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Methyl arachidonate | 99.9% | Methyl arachidonate is a protein kinase C activator and also an orally active substrate that undergoes esterase-mediated hydrolysis. Methyl arachidonate indirectly activates protein kinase C via eicosanoid metabolites generated through the arachidonic acid metabolic pathway, exerting effects via cyclooxygenase products at low concentrations and via lipoxygenase products at high concentrations. Methyl arachidonate can be used in studies related to lipodystrophy. | ||||||||||||||||||||
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- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216. [Content Brief]
- [2]. White, Mary F, et al. The application of the polybromide yield in the estimation of methyl arachidonate in the methyl ester mixtures. Journal of the American Oil Chemists' Society. Volume: 26. Pages: 85-90. Journal.1949.
