Startseite>>(S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide

(S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide

Katalog-Nr.GC91263

Ein Homolog von LOEA

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(S)-(-)-Linoleyl-1'-Hydroxy-2'-Propylamide Chemische Struktur

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1 mg
114,00 $
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5 mg
503,00 $
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10 mg
893,00 $
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

N-Acyl ethanolamines (NAEs) have diverse biological actions that are strongly affected by the associated acyl group. Linoleoyl ethanolamide (LOEA) has potential signaling roles in aging and neurological functioning.1,2 LOEA has a weak affinity for cannabinoid (CB) receptors (Ki = 10 and 25 μM for CB1 and CB2, respectively).3 It also inhibits fatty acid amide drolase (FAAH; Ki = 9 μM) and is drolyzed by FAAH, and inhibits voltage-gated K+ channels.4,5,6 (S)-(−)-Linoleyl-1’-droxy-2’-propylamide is a homolog of LOEA, characterized by the addition of an (S)-α-metl group at the metlene carbon adjacent to the amide nitrogen. A similar modification of arachidonoyl ethanolamide to produce S-1 methanandamide results in a diminished affinity for the CB receptor but greatly improved metabolic stability to aminopeptidase drolysis.7 The psiological actions of this compound have not been evaluated.

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