AM-2201 (original) (raw)

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dbo:abstract AM-2201 (1-(5-fluoropentyl)-3-(1-naphthoyl)indole) is a recreational designer drug that acts as a potent but nonselective full agonist for the cannabinoid receptor. It is part of the AM series of cannabinoids discovered by Alexandros Makriyannis at Northeastern University. (en) AM-2201 ist eine synthetisch hergestellte chemische Verbindung, die zu den Indol-Derivaten und Ketonen zählt. AM-2201 wirkt als synthetisches Cannabinoid auf die Rezeptoren des Endocannabinoid-Systems und entfaltet dort seine Wirkung. Die AM-Serie von Substanzen mit Cannabinoid-Wirkung wurden sämtlich von Alexandros Makriyannis an der Northeastern University erstmals hergestellt. Chemisch hat es eine starke Ähnlichkeit zu JWH-018. Es wird häufig als Rauschmittel gebraucht, da es etwa 30–40 mal potenter als Tetrahydrocannabinol ist. Schon Dosierungen von 250–500 µg zeigen Wirkung. (de) AM-2201、または1-(5-フルオロペンチル)-3-(1-ナフトイル)インドールは、に対する強力だが非選択的な完全作動薬として作用するデザイナードラッグである。のひとつとして、ノースイースタン大学のによって発見された。 (ja) AM-2201 – organiczny związek chemiczny, substancja psychoaktywna z grupy syntetycznych kannabinoidów. Działa jako silny, lecz nieselektywny agonista receptorów kannabinoidowych o Ki 1,0 nM do receptora CB1 oraz 2,6 nM do receptora CB2. Został po raz pierwszy zsyntetyzowany i opatentowany przez grupę , profesora w Bostonie. (pl)
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rdfs:comment AM-2201 (1-(5-fluoropentyl)-3-(1-naphthoyl)indole) is a recreational designer drug that acts as a potent but nonselective full agonist for the cannabinoid receptor. It is part of the AM series of cannabinoids discovered by Alexandros Makriyannis at Northeastern University. (en) AM-2201 ist eine synthetisch hergestellte chemische Verbindung, die zu den Indol-Derivaten und Ketonen zählt. AM-2201 wirkt als synthetisches Cannabinoid auf die Rezeptoren des Endocannabinoid-Systems und entfaltet dort seine Wirkung. Die AM-Serie von Substanzen mit Cannabinoid-Wirkung wurden sämtlich von Alexandros Makriyannis an der Northeastern University erstmals hergestellt. Chemisch hat es eine starke Ähnlichkeit zu JWH-018. Es wird häufig als Rauschmittel gebraucht, da es etwa 30–40 mal potenter als Tetrahydrocannabinol ist. Schon Dosierungen von 250–500 µg zeigen Wirkung. (de) AM-2201、または1-(5-フルオロペンチル)-3-(1-ナフトイル)インドールは、に対する強力だが非選択的な完全作動薬として作用するデザイナードラッグである。のひとつとして、ノースイースタン大学のによって発見された。 (ja) AM-2201 – organiczny związek chemiczny, substancja psychoaktywna z grupy syntetycznych kannabinoidów. Działa jako silny, lecz nieselektywny agonista receptorów kannabinoidowych o Ki 1,0 nM do receptora CB1 oraz 2,6 nM do receptora CB2. Został po raz pierwszy zsyntetyzowany i opatentowany przez grupę , profesora w Bostonie. (pl)
rdfs:label AM-2201 (de) AM-2201 (en) AM-2201 (ja) AM-2201 (pl)
rdfs:seeAlso dbr:JWH-018
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