An analog of N-cyclohexanecarbonylpentadecylamine

N-Cyclohexanecarbonyltetradecylamine – 50 mg

Brand:
Cayman
CAS:
1215071-05-8
Storage:
-20
UN-No:
Non-Hazardous - /

Numerous analogs of fatty acyl ethanolamides potentiate the intrinsic biological activity of endocannabinoids.{10254} This potentiation is ascribed either to inhibition of AEA reuptake into neurons, or inhibition of fatty acid amide hydrolase (FAAH) within the neurons. {10647} However, Ueda, et al. has recently cloned another amidase, the acidic PEAase that promotes the hydrolysis of palmitoylethanolamide.{9989} N-Cyclohexanecarbonyltetradecylamine is an analog of N-cyclohexanecarbonyl-pentadecylamine, a selective inhibitor of acidic PEAase with an IC50 value of 4.5 µM, that contains 1 less carbon in the alkyl chain.{13342} The biological activity of N-cyclohexanecarbonyltetradecylamine has not been documented.  

 

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SKU: 10008317 - 50 mg Category:

Description

An analog of N-cyclohexanecarbonylpentadecylamine, a selective inhibitor of acidic PEAase (IC50 = 4.5 µM), that contains one less carbon in the alkyl chain; its biological activity has not been documented

Formal name: N-tetradecyl-cyclohexanecarboxamide

Synonyms: 

Molecular weight: 323.6

CAS: 1215071-05-8

Purity: ≥98%

Formulation: A crystalline solid

Product Type|Biochemicals|Lipids||Research Area|Lipid Biochemistry|Endocannabinoid/Endocannabinoid-like||Research Area|Neuroscience|Cannabinoid Research|Endocannabinoids

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