142-78-9 | Lauric acid monoethanolamide

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$25.00	$17.00
1g	95%	in stock	$40.00	$28.00
5g	95%	in stock	$60.00	$42.00
10g	95%	in stock	$105.00	$74.00
100g	95%	in stock	$1,006.00	$704.00

Description

• Catalog Number: AB52300
• Chemical Name: Lauric acid monoethanolamide
• CAS Number: 142-78-9
• Molecular Formula: C14H29NO2
• Molecular Weight: 243.3856
• MDL Number: MFCD00020561
• SMILES: CCCCCCCCCCCC(=O)NCCO

Computed Properties

• Complexity: 172
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 12
• Undefined Atom Stereocenter Count: 1
• XLogP3: 4

Literature

• Lauroylethanolamide and linoleoylethanolamide improve functional outcome in a rodent model for stroke.

  Neuroscience letters 20110404

• Effect of head groups on the phase transitions in Gibbs adsorption layers at the air-water interface.

  Journal of colloid and interface science 20100801

• Lauroylethanolamide is a potent competitive inhibitor of lipoxygenase activity.

  FEBS letters 20100716

• The role of N-lauroylethanolamine in the regulation of senescence of cut carnations (Dianthus caryophyllus).

  Journal of plant physiology 20070801

• Synthesis of new plant growth regulator: N-(fatty acid) O-aryloxyacetyl ethanolamine.

  Bioorganic & medicinal chemistry letters 20070601

• Elevated levels of N-lauroylethanolamine, an endogenous constituent of desiccated seeds, disrupt normal root development in Arabidopsis thaliana seedlings.

  Planta 20030601

• Inhibition of phospholipase D alpha by N-acylethanolamines.

  Plant physiology 20020801

• 'Entourage' effects of N-acyl ethanolamines at human vanilloid receptors. Comparison of effects upon anandamide-induced vanilloid receptor activation and upon anandamide metabolism.

  British journal of pharmacology 20020601