| 产品详情 |
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| Product Name | UCM707 |
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| Description | Purity >98%. Numerous analogs of arachidonoyl ethanolamide (AEA, anandamide) potentiate its biological activity. This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. One of the more potent and selective reuptake inhibitors is UCM707, a 3-furyl arachidonoyl analog. UCM707 has an IC50 of 0.8 µM for the inhibition of tritiated AEA uptake into human U937 cells but has low affinity for FAAH, exhibiting an IC50 value of 30 µM. UCM707 also potentiates the biological effects of AEA when co-administered in rats. |
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| Size | n/a |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | N-(3-furanylmethyl)-5Z,8Z,11Z,14Z-eicosatetraenamide |
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| Gene, Accession, CAS # | CAS: 390824-20-1 |
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| Catalog # | LS-H10356 |
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| Order / More Info | UCM707 from LIFESPAN BIOSCIENCES INC. |
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| Product Specific References | n/a |
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| 产品资料 |
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