ANANDAMIDE

ANANDAMIDE Struktur
94421-68-8
CAS-Nr.
94421-68-8
Englisch Name:
ANANDAMIDE
Synonyma:
AEA;ARACHIDONOYL ETHANOLAMIDE;N-ARACHIDONOYLETHANOLAMINE;ARACHIDONYLETHANOLAMIDE;(5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide;8Z;ANANDAMIDE;14-tetraenamide;ANANDAMIDE AEA?;anandamide(20.4,n-6)
CBNumber:
CB7168648
Summenformel:
C22H37NO2
Molgewicht:
347.53
MOL-Datei:
94421-68-8.mol

ANANDAMIDE Eigenschaften

Siedepunkt:
522.3±50.0 °C(Predicted)
Dichte
0.92 g/mL at 25 °C (lit.)
Flammpunkt:
14 °C
storage temp. 
-20°C
Löslichkeit
ethanol: soluble
Aggregatzustand
oil
pka
14.48±0.10(Predicted)
Farbe
light yellow
Wasserlöslichkeit
413ug/L(25 ºC)
Stabilität:
Stable for 1 year from date of purchase as supplied. Subject to oxidation – protect from air. Solutions in degassed DMSO or ethanol may be stored under nitrogen or argon at -80°C for up to 1 month.
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher F
R-Sätze: 11
S-Sätze: 24/25-16-7
RIDADR  UN 1170 3/PG 2
WGK Germany  3
RTECS-Nr. JX3842500
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H314 Verursacht schwere Verätzungen der Haut und schwere Augenschäden. Ätzwirkung auf die Haut Kategorie 1B Achtung GHS hazard pictogramssrc="/GHS05.jpg" width="20" height="20" /> P260,P264, P280, P301+P330+ P331,P303+P361+P353, P363, P304+P340,P310, P321, P305+ P351+P338, P405,P501
Sicherheit
P271 Nur im Freien oder in gut belüfteten Räumen verwenden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P330+P331 BEI VERSCHLUCKEN: Mund ausspülen. KEIN Erbrechen herbeiführen.
P304+P340 BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P310 Sofort GIFTINFORMATIONSZENTRUM/Arzt/ anrufen.
P363 Kontaminierte Kleidung vor erneutem Tragen waschen.
P403+P233 An einem gut belüfteten Ort aufbewahren. Behälter dicht verschlossen halten.

ANANDAMIDE Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R11:Leichtentzündlich.

S-Sätze Betriebsanweisung:

S24/25:Berührung mit den Augen und der Haut vermeiden.
S16:Von Zündquellen fernhalten - Nicht rauchen.
S7:Behälter dicht geschlossen halten.

Definition

ChEBI: An N-(polyunsaturated fatty acyl)ethanolamine resulting from the formal condensation of carboxy group of arachidonic acid with amino group of ethanolamine.

Hazard

A reproductive hazard.

Biologische Aktivität

Endogenous cannabinoid and vanilloid receptor agonist, in water-soluble emulsion (for details see TocrisolveTM 100). K i values are 89 and 371 nM for CB 1 and CB 2 receptors respectively; EC 50 values are 18, 31 and 27 nM at GPR55, CB 1 and CB 2 respectively; pK i = 5.68 for rVR1. Also blocks TNF- α -induced NF-kB activation via direct inhibition of IKK. Also available as the pure oil dissolved in ethanol (N-(2-Hydroxyethyl)-5Z,8Z,11Z,14Z-eicosatetraenamide ).

Enzyminhibitor

This lipid neurotransmitter and endocannabinoid receptor ligand (FW = 347.54 g/mol; CAS 94421-68-8), also known as arachidonylethanolamide, inhibits calcium ion currents and activates the MAP kinase signaling pathway. Anandamide is a naturally occurring effector of central and peripheral nervous systems, as mediated by CB1 and CB2 cannabinoid receptors, respectively. (These receptors were originally characterized as binding Δ9 -tetrahydrocannabinol, or THC, marijuana’s major psychoactive ingredient.) Anandamide, 2-arachidonoylglycerol, and congeners (N- oleoylethanolamide and N-palmitoylethanolamide) are lipophilic signalling molecules with multiple physiological roles in learning and memory, neuroinflammation, oxidative stress, neuroprotection and neurogenesis. Anandamide likewise plays a role in regulating uterine implantation of the early-stage embryo (blastocyst). Anandamide synthesis occurs from N- acetylphosphatidylethanolamine by multiple pathways that include phospholipase A2, phospholipase C, and NAPE-hydrolyzing phospholipase D (or NAPE-PLD). Target(s): adenylate cyclase; Na + channels; a7-nicotinic acetylcholine receptor; 5 HT3 receptors; Ca 2+ channels; K+ channels, voltage-gated; acylglycerol lipase, or monoacylglycerol lipase.

ANANDAMIDE Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


ANANDAMIDE Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 79)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 19892 58
Shanghai UCHEM Inc.
+862156762820 +86-13564624040
sales@myuchem.com China 6711 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471
sales@sarms4muscle.com China 10523 58
Hong Kong Tiansheng New Material Trading Co., Ltd
+8617320695765
zxx@hktiansheng.com China 981 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418684 +8618949823763
sales@tnjchem.com China 25363 58
Hebei baicao biology science and technology co., ltd
+86-19131911055 +8617824879454
zhang@hbbocao.com China 1035 58
Hebei Linwo New Material Technology Co., LTD
+8618134091113
sales5@hblwxcl.com China 991 58
Hebei Miaoyin Technology Co.,Ltd
+86-17367732028 +86-17367732028
kathy@hbyinsheng.com China 3582 58
Shaanxi LonierHerb Bio Technology Co Ltd
+86-86-+86-86-029-87551862 +8617702909819
sales006@ingredients-lonier.com China 2596 58
Henan Bao Enluo International TradeCo.,LTD
+86-17331933971 +86-17331933971
deasea125996@gmail.com China 2503 58

94421-68-8()Verwandte Suche:


  • Arachidonylethanolamide,AEA, Anandamide, Arachidonic acid N-(hydroxyethyl)amide
  • Anandamide (in Tocrisolve 100)
  • Arachidonoyl Ethanolamide Lipid Maps MS Standard
  • (5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)-5,8,11,14-eicosatetraenamide
  • ARACHIDONYLETHANOLAMIDE, >=97.0% (TL
  • 11,14-eicosatetraenamide(all-z)-n-(2-hydroxyethyl)-8
  • 14-eicosatetraenamide,n-(2-hydroxyethyl)-(all-z)-11
  • 5,8,11,14-eicosatetraenoylethanolamide
  • anandamide(20.4,n-6)
  • n-(2-hydroxyethyl)anachidonamide
  • n-arachidonoyl-2-hydroxyethylamide
  • ARACHIDONIC ACID N-[HYDROXYETHYL]AMIDE
  • 5,8,11,14(Z,Z,Z,Z)-EICOSATETRAENOYL 2'-HYDROXYETHYL-AMIDE
  • ANANDAMIDE
  • N-(2-HYDROXYETHYL)-5Z,8Z,11Z,14Z-EICOSATETRAENAMIDE
  • Anandamide(inTocrisolveTM100)
  • AEA, Anandamide, Arachidonic acid N-(hydroxyethyl)amide
  • 5,8,11,14-Eicosatetraenamide, N-(2-hydroxyethyl)-, (5Z,8Z,11Z,14Z)-
  • 5,8,11,14-Eicosatetraenamide, N-(2-hydroxyethyl)-, (all-Z)-
  • N-(2-Hydroxyethyl)-5,8,11,14-eicosatetraenamide (all-Z)-
  • Arachidonoyl Ethanolamide (in ethanol)
  • Arachidonoyl Ethanolamide MaxSpecStandard
  • ANANDAMIDE/AEA Powder
  • Anandamide CAS 94421 68 8
  • (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenami...
  • 14-tetraenamide
  • 14Z)-N-(2-Hydroxyethyl)icosa-5
  • 8Z
  • ARACHIDONOYL ETHANOLAMIDE
  • ARACHIDONYLETHANOLAMIDE
  • AEA
  • N-ARACHIDONOYLETHANOLAMINE
  • (5Z,8Z,11Z,14Z)-N-(2-hydroxyethyl)icosa-5,8,11,14-tetraenamide
  • Transient receptor potential channels,Inhibitor,inhibit,Alzheimer’s disease,Candida albicans,Anandamide,anti-fungal,anti-adhesive,cervical epithelial cells,Endogenous Metabolite,G protein-coupled receptor 55,Streptozotocin,hVSMC,HeLa cells,GPR55,TRP Channel,Cannabinoid Receptor,endocannabinoid,Peroxisome proliferator-activated receptors,Fungal,PPAR,Tau Protein
  • ANANDAMIDE AEA?
  • 94421-68-8
  • C22H37NO2
  • Unsaturated fatty acids and derivatives
  • Polyunsaturated
  • Lipids
  • Fatty Acids
  • Fatty acid amides
  • BioChemical
  • Biochemicals and Reagents
  • Cannabinoid receptor
  • Cannabinoid
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