AL-38022A
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AL-38022A
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| Systematic (IUPAC) name | |
| (S)-2-(8,9-dihydro-7H-pyrano[2,3-g]indazol-1-yl)-1-methylethylamine | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| ATC code | ? |
| PubChem | CID 22496603 |
| ChemSpider | 26286943 |
| Chemical data | |
| Formula | C13H17N3O |
| Mol. mass | 231.293 g/mol |
| SMILES | eMolecules & PubChem |
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| Physical data | |
| Melt. point | 106–107 °C (223–225 °F) |
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AL-38022A is an indazole derivative drug which is one of a range of similar drugs developed for scientific research and with some possible clinical applications. It acts as a potent and selective agonist for the 5-HT2 family of serotonin receptors, with highest binding affinity for the 5-HT2C subtype and around 4x less affinity for 5-HT2A and 5-HT2B. In drug discrimination tests on animals, it fully substituted for both DOM and 5-MeO-DMT.[1]
See also
References
- ^ May, JA; Sharif, NA; Chen, HH; Liao, JC; Kelly, CR; Glennon, RA; Young, R; Li, JX et al (2009). "Pharmacological properties and discriminative stimulus effects of a novel and selective 5-HT2 receptor agonist AL-38022A (S)-2-(8,9-dihydro-7H-pyrano2,3-gindazol-1-yl)-1-methylethylamine". Pharmacology, Biochemistry, and Behavior 91 (3): 307–14. doi:10.1016/j.pbb.2008.07.015. PMID 18718483.
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