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- AM-1221 abstract "AM-1221 is a drug that acts as a potent and selective agonist for the cannabinoid receptor CB2, with a Ki of 0.28nM at CB2 and 52.3nM at the CB1 receptor, giving it around 180x selectivity for CB2. The 2-methyl and 6-nitro groups on the indole ring both tend to increase CB2 affinity while generally reducing affinity at CB1, explaining the high CB2 selectivity of AM-1221. However, despite this relatively high selectivity for CB2, its CB1 affinity is still too strong to make it useful as a truly selective CB2 agonist, so the related compound AM-1241 is generally preferred for research purposes.".
- AM-1221 casNumber "335160-53-7".
- AM-1221 fdaUniiCode "SHC6SNM293".
- AM-1221 iupacName "1-[(N-methylpiperidin-2-yl)methyl]-2-methyl-3-(naphthalen-1-oyl)-6-nitroindole".
- AM-1221 pubchem "11604318".
- AM-1221 thumbnail AM-1221_structure.png?width=300.
- AM-1221 wikiPageID "30438367".
- AM-1221 wikiPageLength "4082".
- AM-1221 wikiPageOutDegree "24".
- AM-1221 wikiPageRevisionID "708315041".
- AM-1221 wikiPageWikiLink AM-1220.
- AM-1221 wikiPageWikiLink AM-1235.
- AM-1221 wikiPageWikiLink AM-1241.
- AM-1221 wikiPageWikiLink AM-2233.
- AM-1221 wikiPageWikiLink AM-630.
- AM-1221 wikiPageWikiLink Agonist.
- AM-1221 wikiPageWikiLink Cannabinoid_receptor.
- AM-1221 wikiPageWikiLink Cannabinoid_receptor_type_1.
- AM-1221 wikiPageWikiLink Cannabinoid_receptor_type_2.
- AM-1221 wikiPageWikiLink Category:AM_cannabinoids.
- AM-1221 wikiPageWikiLink Category:Aminoalkylindoles.
- AM-1221 wikiPageWikiLink Category:CB1_receptor_agonists.
- AM-1221 wikiPageWikiLink Category:CB2_receptor_agonists.
- AM-1221 wikiPageWikiLink Category:Cannabinoids.
- AM-1221 wikiPageWikiLink Category:Designer_drugs.
- AM-1221 wikiPageWikiLink Category:Naphthoylindoles.
- AM-1221 wikiPageWikiLink Category:Nitrobenzenes.
- AM-1221 wikiPageWikiLink Category:Piperidines.
- AM-1221 wikiPageWikiLink Dissociation_constant.
- AM-1221 wikiPageWikiLink Indole.
- AM-1221 wikiPageWikiLink Methyl_group.
- AM-1221 wikiPageWikiLink N-(S)-Fenchyl-1-(2-morpholinoethyl)-7-methoxyindole-3-carboxamide.
- AM-1221 wikiPageWikiLink Nitro_compound.
- AM-1221 wikiPageWikiLink UR-144.
- AM-1221 wikiPageWikiLinkText "AM-1221".
- AM-1221 c "27".
- AM-1221 casNumber "335160".
- AM-1221 chemspiderid "26286945".
- AM-1221 h "27".
- AM-1221 inchi "1".
- AM-1221 inchikey "QGNIEJBBHMMNOZ-UHFFFAOYAI".
- AM-1221 iupacName "1".
- AM-1221 legalCa "Schedule II".
- AM-1221 molecularWeight "441.521".
- AM-1221 n "3".
- AM-1221 o "3".
- AM-1221 pubchem "11604318".
- AM-1221 smiles "c5ccc2ccccc2c5Cccn1CC3CCCCN3C".
- AM-1221 stdinchi "1".
- AM-1221 stdinchikey "QGNIEJBBHMMNOZ-UHFFFAOYSA-N".
- AM-1221 unii "SHC6SNM293".
- AM-1221 verifiedfields "changed".
- AM-1221 verifiedrevid "462655327".
- AM-1221 width "200".
- AM-1221 wikiPageUsesTemplate Template:Cannabinoid-stub.
- AM-1221 wikiPageUsesTemplate Template:Cannabinoids.
- AM-1221 wikiPageUsesTemplate Template:Cascite.
- AM-1221 wikiPageUsesTemplate Template:Chemspidercite.
- AM-1221 wikiPageUsesTemplate Template:Drugbankcite.
- AM-1221 wikiPageUsesTemplate Template:Drugbox.
- AM-1221 wikiPageUsesTemplate Template:Fdacite.
- AM-1221 wikiPageUsesTemplate Template:Reflist.
- AM-1221 wikiPageUsesTemplate Template:Stdinchicite.
- AM-1221 subject Category:AM_cannabinoids.
- AM-1221 subject Category:Aminoalkylindoles.
- AM-1221 subject Category:CB1_receptor_agonists.
- AM-1221 subject Category:CB2_receptor_agonists.
- AM-1221 subject Category:Cannabinoids.
- AM-1221 subject Category:Designer_drugs.
- AM-1221 subject Category:Naphthoylindoles.
- AM-1221 subject Category:Nitrobenzenes.
- AM-1221 subject Category:Piperidines.
- AM-1221 hypernym Drug.
- AM-1221 type ChemicalSubstance.
- AM-1221 type Drug.
- AM-1221 type Cannabinoid.
- AM-1221 type Drug.
- AM-1221 type Heterocycle.
- AM-1221 type Ketone.
- AM-1221 type ChemicalObject.
- AM-1221 type Thing.
- AM-1221 type Q8386.
- AM-1221 comment "AM-1221 is a drug that acts as a potent and selective agonist for the cannabinoid receptor CB2, with a Ki of 0.28nM at CB2 and 52.3nM at the CB1 receptor, giving it around 180x selectivity for CB2. The 2-methyl and 6-nitro groups on the indole ring both tend to increase CB2 affinity while generally reducing affinity at CB1, explaining the high CB2 selectivity of AM-1221.".
- AM-1221 label "AM-1221".
- AM-1221 sameAs Q4652482.
- AM-1221 sameAs m.0g5s2zt.
- AM-1221 sameAs AM-1221.
- AM-1221 sameAs AM-1221.
- AM-1221 sameAs Q4652482.
- AM-1221 wasDerivedFrom AM-1221?oldid=708315041.
- AM-1221 depiction AM-1221_structure.png.
- AM-1221 isPrimaryTopicOf AM-1221.