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フォーム
powder
包装
pkg of 1 × 5 mg (870431P-5mg)
メーカー／製品名
Avanti Research™ - A Croda Brand 870431P
脂質タイプ
bioactive lipids
輸送温度
dry ice
保管温度
−20°C
SMILES記法
O=C(CCCCCCCC/C=C\CCCCCC)NCCO
詳細
C17:1 anandamide, also known as 10Z-heptadecenoylethanolamide, is a N-acyl ethanolamide derivative of heptadecanoic acid.
アプリケーション
C17:1 anandamide or 10Z-heptadecenoylethanolamide has been used as an internal standard in mass spectrometry analysis for the measurement of 2-arachidonoyl glycerol (2-AG) in brain tissue. It has also been used as a substrate for N-acylethanolamine acid amidase (NAAA) enzyme.
包装
5 mL Clear Glass Sealed Ampule (870431P-5mg)
法的情報
Avanti Research is a trademark of Avanti Polar Lipids, LLC
保管分類コード
11 - Combustible Solids
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
870431P-5MG:
870431P-VAR:
870431P-BULK:
最新バージョンのいずれかを選択してください：
Yoki Nakamura et al.
eLife, 8 (2019-10-10)
Cocaine is an addictive drug that acts in brain reward areas. Recent evidence suggests that cocaine stimulates synthesis of the endocannabinoid 2-arachidonoylglycerol (2-AG) in midbrain, increasing dopamine neuron activity via disinhibition. Although a mechanism for cocaine-stimulated 2-AG synthesis is known
Oscar Sasso et al.
Pain, 154(3), 350-360 (2012-12-12)
Fatty acid ethanolamides (FAEs), which include palmitoylethanolamide (PEA) and oleoylethanolamide (OEA), are endogenous agonists of peroxisome proliferator-activated receptor-α (PPAR-α) and important regulators of the inflammatory response. They are degraded in macrophages by the lysosomal cysteine amidase, N-acylethanolamine acid amidase (NAAA).
Natsuo Ueda et al.
Biochimica et biophysica acta, 1801(12), 1274-1285 (2010-08-26)
Ethanolamides of different long-chain fatty acids constitute a class of endogenous lipid molecules generally called N-acylethanolamines (NAEs). They contain N-arachidonoylethanolamine (anandamide), N-palmitoylethanolamine, and N-oleoylethanolamine, which receive considerable attention because of their actions as an endogenous cannabinoid receptor ligand (endocannabinoid), an
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