11-Methoxyasimilobine

Pharmaceutical compound From Wikipedia, the free encyclopedia

11-Methoxyasimilobine, also known as 1,11-dimethoxy-2-hydroxynoraporphine, is a serotonin 5-HT2 receptor agonist of the noraporphine family related to the noraporphine alkaloid asimilobine.[1][2] It is the 11-methoxy derivative of asimilobine.[1][2]

Other names1,11-Dimethoxy-2-hydroxynoraporphine; Compound 16l; Compound S31
ATC code
  • None
Quick facts Clinical data, Other names ...
11-Methoxyasimilobine
Clinical data
Other names1,11-Dimethoxy-2-hydroxynoraporphine; Compound 16l; Compound S31
Drug classSerotonin 5-HT2 receptor agonist; Serotonin 5-HT2A receptor agonist; Serotonin 5-HT2C receptor agonist
ATC code
  • None
Identifiers
  • 1,11-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol
PubChem CID
Chemical and physical data
FormulaC18H19NO3
Molar mass297.354 g·mol−1
3D model (JSmol)
  • COC1=CC=CC2=C1C3=C4C(C2)NCCC4=CC(=C3OC)O
  • InChI=1S/C18H19NO3/c1-21-14-5-3-4-10-8-12-15-11(6-7-19-12)9-13(20)18(22-2)17(15)16(10)14/h3-5,9,12,19-20H,6-8H2,1-2H3
  • Key:IRZSTYZUXGRZIR-UHFFFAOYSA-N
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Whereas asimilobine is a selective, lower-potency, high-efficacy partial agonist of the serotonin 5-HT2C receptor,[3] 11-methoxyasimilobine is a highly potent and selective full agonist of both the serotonin 5-HT2A and 5-HT2C receptors, with approximately 8-fold preferential activation of the serotonin 5-HT2C receptor over the serotonin 5-HT2A receptor.[1] Its EC50Tooltip half-maximal effective concentration (EmaxTooltip maximal efficacy) values were 18 nM (98%) at the serotonin 5-HT2A receptor and 2.3 nM (100%) at the serotonin 5-HT2C receptor.[1] The drug is a biased agonist of the serotonin 5-HT2C receptor, favoring Gq signaling over β-arrestin recruitment by approximately 6.3-fold.[1] It was among the most potent dual serotonin 5-HT2A and 5-HT2C receptor agonists of a large series of assessed noraporphines.[1]

Besides the serotonin 5-HTA and 5-HT2C receptors, the drug also showed weak agonism of the serotonin 5-HT2B receptor, but only at very high concentrations (EC50 = >10,000 nM).[1][2] It showed little activity at a selection of other serotonin receptors.[1]

The chemical synthesis of 11-methoxyasimilobine has been described.[1][2] A variety of analogues of the drug with similar activity have also been described.[1][2]

11-Methoxyasimilobine was described in the scientific literature by Wangzhi Qin and colleagues in 2025.[1] It had previously been patented in 2022.[2] There is interest in 11-methoxyasimilobine and related compounds for potential medical use, such as treatment of anxiety, obsessive–compulsive disorder (OCD), and substance use disorders.[1][2]

See also

References

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