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| | (±)11(12)-EET-d11 methyl ester Basic information |
| | (±)11(12)-EET-d11 methyl ester Chemical Properties |
| solubility | DMF: >50 mg/ml
DMSO: >50 mg/ml
Ethanol: >50 mg/mlPBS (pH 7.2): >1mg/ml |
| | (±)11(12)-EET-d11 methyl ester Usage And Synthesis |
| Description | (±)11(12)-EET-d11 methyl ester is intended for use as an internal standard for the quantification of 11(12)-EET methyl ester by GC- or LC-MS. 11(R),12(S)-EET and 11(S),12(R)-EET are formed via epoxidation of arachidonic acid (Item Nos. 90010 | 90010.1 | 10006607) by a variety of cytochrome P450 (CYP) isoforms.1 11(R),12(S)-EET is produced at a higher proportion by CYP2C8, CYP2C23, and CYP2C24 isoforms, whereas 11(S),12(R)-EET is produced at a greater proportion by CYP2B2 and CYP2C10 isoforms.2,1WARNING This product is not for human or veterinary use. | | References | [1] ARTHUR A SPECTOR A W N. Action of epoxyeicosatrienoic acids on cellular function.[J]. American journal of physiology. Cell physiology, 2007, 292 3: C996-1012. DOI: 10.1152/ajpcell.00402.2006
[2] J H CAPDEVILA R C H J R Falck. Cytochrome P450 and arachidonic acid bioactivation. Molecular and functional properties of the arachidonate monooxygenase.[J]. Journal of Lipid Research, 2000, 41 2: 163-181.
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| | (±)11(12)-EET-d11 methyl ester Preparation Products And Raw materials |
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