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| | (14(15)-DiHET-d11 Basic information |
| Product Name: | (14(15)-DiHET-d11 | | Synonyms: | (14(15)-DiHET-d11;(±)14(15)-DiHET-d11 | | CAS: | | | MF: | C20H23D11O4 | | MW: | 349.549339558 | | EINECS: | | | Product Categories: | | | Mol File: | Mol File |  |
| | (14(15)-DiHET-d11 Chemical Properties |
| solubility | DMF: 50 mg/ml
DMSO: 50 mg/ml
Ethanol: 50 mg/mlPBS (pH 7.2): 0.5 mg/ml |
| | (14(15)-DiHET-d11 Usage And Synthesis |
| Description | (±)14,15-DiHET-d11 is intended for use as an internal standard for the quantification of 14(15)-DiHET by GC- or LC-MS. 14(R),15(R)-DiHET and 14(S),15(S)-DiHET are vicinal diols formed via enzymatic hydration of 14(15)-EET by cytosolic or soluble epoxide hydrolases.1,2 14(R),15(R)-DiHET is produced at a greater proportion than 14(S),15(S)-DiHET by cytosolic epoxide hydrolase.1WARNING This product is not for human or veterinary use. | | References | [1] D C ZELDIN. Regio- and enantiofacial selectivity of epoxyeicosatrienoic acid hydration by cytosolic epoxide hydrolase.[J]. The Journal of Biological Chemistry, 1993, 268 9: 6402-6407.
[2] GUODONG ZHANG Bruce D H Sean Kodani. Stabilized epoxygenated fatty acids regulate inflammation, pain, angiogenesis and cancer[J]. Progress in lipid research, 2014, 53: Pages 108-123. DOI: 10.1016/j.plipres.2013.11.003 |
| | (14(15)-DiHET-d11 Preparation Products And Raw materials |
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