(±)17(18)-EpETE-Ethanolamide

(±)17(18)-EpETE-Ethanolamide
Item number Size Datasheet Manual SDS Delivery time Quantity Price
Cay25920-25 25 µg -

6 - 10 business days*

57.00€
Cay25920-50 50 µg -

6 - 10 business days*

107.00€
Cay25920-100 100 µg -

6 - 10 business days*

199.00€
Cay25920-500 500 µg -

6 - 10 business days*

879.00€
 
(±)17(18)-EpETE-Ethanolamide is an omega-3 endocannabinoid epoxide. It is formed from the... more
Product information "(±)17(18)-EpETE-Ethanolamide"
(±)17(18)-EpETE-Ethanolamide is an omega-3 endocannabinoid epoxide. It is formed from the endocannabinoid eicosapentaenoic ethanolamide (EPEA) via cytochrome P450 (CYP) epoxygenases and hydrolyzed by soluble epoxide hydrolase (sEH) and fatty acid amide hydrolase (FAAH). It is endogenously produced in LPS-stimulated BV-2 microglia cells and in BV-2 microglia cells supplemented with EPEA, an effect that can be reduced by the CYP inhibitor ketoconazole. (±)17(18)-EpETE-ethanolamide decreases IL-6 and nitrite production induced by LPS in BV-2 microglia and increases the production of IL-10. It inhibits platelet aggregation induced by arachidonic acid (Cay-90010, Cay-90010.1, Cay-10006607) when used at a concentration of 50 µM but not aggregation induced by ADP (Cay-16778, Cay-21121), collagen, or ristocetin. It also induces relaxation of preconstricted bovine coronary arteries (ED50 = 1.1 µM) and inhibits VEGF-stimulated tubulogenesis in human microvascular endothelial cells (HMVECs). (±)17(18)-EpETE-ethanolamide is the predominant EPEA metabolite found in rat brain, and it has also been found in rat heart, kidney, spleen, and liver, as well as in pig brain. It activates cannabinoid receptor 1 (CB1) and CB2 with EC50 values of 18.5 and 1.4 nM, respectively, in a beta-arrestin recruitment assay.Formal Name: 16-(3-ethyl-2-oxiranyl)-N-(2-hydroxyethyl)-5Z,8Z,11Z,14Z-hexadecatetraenamide. CAS Number: 2123491-23-4. Synonyms: 17,18-EEQ-EA, (±)17,18-EEQ-Ethanolamide, (±)17(18)-EpETE-EA, 17,18-epoxy-Eicosatetraenoic Acid Ethanolamide. Molecular Formula: C22H35NO3. Formula Weight: 361.5. Purity: >98%. Formulation: (Request formulation change), A solution in ethanol. Solubility: DMF: 30 mg/ml, DMSO: 25 mg/ml, Ethanol: 30 mg/ml. SMILES: CCC1C(O1)C/C=C\C/C=C\C/C=C\C/C=C\CCCC(NCCO)=O. InChi Code: InChI=1S/C22H35NO3/c1-2-20-21(26-20)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-22(25)23-18-19-24/h3,5-6,8-9,11-12,14,20-21,24H,2,4,7,10,13,15-19H2,1H3,(H,23,25)/b5-3-,8-6-,11-9-,14-12-. InChi Key: PVTVBNICUOQEDT-JPURVOHMSA-N.
Keywords: 17,18-EEQ-EA, (±)17(18)-EpETE-EA, (±)17,18-EEQ-Ethanolamide, 17,18-epoxy-Eicosatetraenoic Acid Ethanolamide, 16-(3-ethyl-2-oxiranyl)-N-(2-hydroxyethyl)-5Z,8Z,11Z,14Z-hexadecatetraenamide
Supplier: Cayman Chemical
Supplier-Nr: 25920

Properties

Application: omega-3 endocannabinoid epoxide, soluble epoxide hydrolase (sEH) & FAAH substrate
MW: 361.5 D
Formula: C22H35NO3
Purity: >98%
Format: Solution

Database Information

CAS : 2123491-23-4| Matching products
KEGG ID : K15528 | Matching products

Handling & Safety

Storage: -20°C
Shipping: -20°C (International: -20°C)
Signal Word: Danger
GHS Hazard Pictograms:
H Phrases: H225, H319
P Phrases: P210, P233, P240, P241, P242, P243, P264, P280, P303+361+353, P305+351+338, P337+313, P370+378, P403+235, P501
Caution
Our products are for laboratory research use only: Not for administration to humans!
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