Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H31NO2 |
| Molecular Weight | 257.4121 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCCCC(=O)NCC(C)O
InChI
InChIKey=MMBILEWCGWTAOV-UHFFFAOYSA-N
InChI=1S/C15H31NO2/c1-3-4-5-6-7-8-9-10-11-12-15(18)16-13-14(2)17/h14,17H,3-13H2,1-2H3,(H,16,18)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effect of head groups on the phase transitions in Gibbs adsorption layers at the air-water interface. | 2010-08-01 |
|
| Lauroylethanolamide is a potent competitive inhibitor of lipoxygenase activity. | 2010-07-16 |
|
| 'Entourage' effects of N-acyl ethanolamines at human vanilloid receptors. Comparison of effects upon anandamide-induced vanilloid receptor activation and upon anandamide metabolism. | 2002-06 |
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82DUX3RRVU
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205-541-8
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9903249
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82DUX3RRVU
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DTXSID00861815
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142-54-1
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2262541
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SUBSTANCE RECORD
