AM-1221

Source: Wikipedia, the free encyclopedia.
AM-1221
Legal status
Legal status
Identifiers
  • 1-[(N-Methylpiperidin-2-yl)methyl]-2-methyl-3-(naphthalen-1-oyl)-6-nitroindole
JSmol)
  • CN1CCCCC1CN2C=C(C3=C2C=C(C=C3)[N+](=O)[O-])C(=O)C4=CC=CC5=CC=CC=C54
  • InChI=1S/C27H27N3O3/c1-18-26(27(31)23-12-7-9-19-8-3-4-11-22(19)23)24-14-13-20(30(32)33)16-25(24)29(18)17-21-10-5-6-15-28(21)2/h3-4,7-9,11-14,16,21H,5-6,10,15,17H2,1-2H3 checkY
  • Key:QGNIEJBBHMMNOZ-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

AM-1221 is a drug that acts as a potent and selective

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.[2][3]

In the United States, all CB1 receptor agonists of the 3-(1-naphthoyl)indole class such as AM-1221 are

Legal status

It is illegal to supply, trade, sell, distribute, import or transport the pharmaceutical drug in the UK under the Psychoactive Substances Act 2016 which was in force on May 26, 2016.

See also

References

  1. Makriyannis A
    , Deng H, "Cannabimimetic indole derivatives", granted 2001-06-07 
  2. ProQuest 304624325
    .
  3. .
  4. ^ 21 U.S.C. § 812: Schedules of controlled substances