AM-630
Systematic (IUPAC) name | |
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1-[2-(morpholin-4-yl)ethyl]-2-methyl-3-(4-methoxybenzoyl)-6-iodoindole
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Clinical data | |
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Identifiers | |
CAS Number | 164178-33-0 |
PubChem | CID: 4302963 |
IUPHAR/BPS | 750 |
ChemSpider | 3508738 |
ChEMBL | CHEMBL181633 |
Chemical data | |
Formula | C23H25IN2O3 |
Molecular mass | 504.360 g/mol |
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AM-630 (6-Iodopravadoline) is a drug that acts as a potent and selective inverse agonist for the cannabinoid receptor CB2, with a Ki of 32.1nM at CB2 and 165x selectivity over CB1, at which it acted as a weak partial agonist.[1][2] It is used in the study of CB2 mediated responses and has been used to investigate the possible role of CB2 receptors in the brain.[3][4] AM-630 is significant as one of the first indole derived cannabinoid ligands substituted on the 6-position of the indole ring, a position that has subsequently been found to be important in determining affinity and efficacy at both the CB1 and CB2 receptors, and has led to the development of a large number of related derivatives.[5][6][7][8][9]
See also
- WIN 48,098 (Pravadoline)
- WIN 54,461 (6-Bromopravadoline)
- AM-1221
References
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- ↑ Hongfeng Deng. Design and synthesis of selective cannabinoid receptor ligands: Aminoalkylindole and other heterocyclic analogs. PhD Dissertation, University of Connecticut, 2000.
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- Cannabinoids
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