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Docosahexaenoyl Ethanolamide-d4 Sale

(Synonyms: Dehydroepiandrosteron(DHEA)-d4; Docosahexaenoyl ethanolamide-d4) 目录号 : GC47253

An internal standard for the quantification of docosahexaenoyl ethanolamide

Docosahexaenoyl Ethanolamide-d4 Chemical Structure

Cas No.:946524-43-2

规格 价格 库存 购买数量
500 μg
¥839.00
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1 mg
¥1,593.00
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5 mg
¥6,716.00
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10 mg
¥11,751.00
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Sample solution is provided at 25 µL, 10mM.

Description

Docosahexaenoyl ethanolamide-d4 contains four deuterium atoms at the 1, 1', 2, and 2' positions. It is intended for use as an internal standard for the quantification of docosahexaenoyl ethanolamide by GC- or LC-mass spectrometry (MS). Docosahexaenoic Acid (DHA) is an essential fatty acid and the most abundant ω-3 fatty acid in neural tissues, especially in the retina and brain. Docosahexaenoyl ethanolamide (DHEA) is the ethanolamine amide of DHA that has been detected in both brain and retina at concentrations similar to those for arachidonoyl ethanolamide (AEA).1,2 A 9.5 fold increase of DHEA was observed in brain lipid extracts from piglets fed a diet supplemented with DHA compared to a control diet without DHA.3 DHEA binds to the rat brain CB1 receptor with a Ki value of 324 nM, which is approximately 10-fold higher than the Ki value for AEA.4 DHEA inhibits shaker-related voltage-gated potassium channels in brain slightly better than AEA, with an IC50 value of 1.5 µM.5

1.Sugiura, T., Kondo, S., Sukagawa, A., et al.Transacylase-mediated and phosphodiesterase-mediated synthesis of N-arachidonoylethanolamine, an endogenous cannabinoid-receptor ligand, in rat brain microsomes. Comparison with synthesis from free arachidonic acid and ethanolamineEuropean Journal of Biochemistry24053-62(1996) 2.Bisogno, T., Delton-Vandenbroucke, I., Milone, A., et al.Biosynthesis and inactivation of N-Arachidonoylethanolamine (Ananadamide) and N-Docosahexaenoylethanolamine in bovine retinaArchives of Biochemistry and Biophysics370(2)300-307(1999) 3.Berger, A., Crozier, G., Bisogno, T., et al.Anandamide and diet: Inclusion of dietary arachidonate and docosahexaenoate leads to increased brain levels of the corresponding N-acylethanolamines in pigletsProceedings of the National Academy of Sciences of the United States of America98(11)6402-6406(2001) 4.Sheskin, T., Hanus, L., Slager, J., et al.Structural requirements for binding of anandamide-type compounds to the brain cannabinoid receptorJournal of Medicinal Chemistry40659-667(1997) 5.Poling, J.S., Rogawski, M.A., Salem, N., Jr., et al.Anadamide, an endogenous cannabinoid, inhibits shaker-related voltage-gated K+ channelsNeuropharmacology35(7)983-991(1996)

化学性质

Cas No. 946524-43-2 SDF
别名 Dehydroepiandrosteron(DHEA)-d4; Docosahexaenoyl ethanolamide-d4
Canonical SMILES O=C(NC([2H])([2H])C([2H])([2H])O)CC/C=C\C/C=C\C/C=C\C/C=C\C/C=C\C/C=C\CC
分子式 C24H33D4NO2 分子量 375.6
溶解度 DMF: 20 mg/ml,DMSO: 20 mg/ml,Ethanol: 5 mg/ml,PBS (pH 7.2): 0.15 mg/ml 储存条件 Store at -20°C
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储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至37℃,然后在超声波浴中震荡一段时间。
Shipping Condition 评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备RT,或根据请求配备蓝冰。

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.6624 mL 13.312 mL 26.6241 mL
5 mM 0.5325 mL 2.6624 mL 5.3248 mL
10 mM 0.2662 mL 1.3312 mL 2.6624 mL
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