Org 27569

Org 27569

Systematic (IUPAC) name
5-chloro-3-ethyl-1H-indole-2-carboxylic acid [2-(4-piperidin-1-yl-phenyl)ethyl]amide
Identifiers
CAS Number	868273-06-7
PubChem	CID 44828492
IUPHAR/BPS	7851
ChemSpider	22369629
Chemical data
Formula	C24H28ClN3O
Molar mass	409.951 g/mol
SMILES CCc1c2cc(Cl)ccc2nc1C(=O)NCCc3ccc(cc3)N4CCCCC4
InChI InChI=1S/C24H28ClN3O/c1-2-20-21-16-18(25)8-11-22(21)27-23(20)24(29)26-13-12-17-6-9-19(10-7-17)28-14-4-3-5-15-28/h6-11,16,27H,2-5,12-15H2,1H3,(H,26,29) Key:AHFZDNYNXFMRFQ-UHFFFAOYSA-N
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Org 27569 is a drug which acts as a potent and selective positive allosteric modulator of the cannabinoid CB₁ receptor. Studies in vitro suggest that it binds to a regulatory site on the CB₁ receptor target, causing a conformational change that increases the binding affinity of CB₁ agonists such as CP 55,940, while decreasing the binding affinity of CB₁ antagonists or inverse agonists such as rimonabant. However while Org 27569 increases the ability of CB₁ agonists to bind to the receptor, it decreases their efficacy at stimulating second messenger signalling once bound, and so in practice behaves as an insurmountable antagonist of CB₁ receptor function.^[1]

See also

• GAT100
• PSNCBAM-1
• ZCZ-011

References

1. Price MR, Baillie GL, Thomas A, Stevenson LA, Easson M, Goodwin R, McLean A, McIntosh L, Goodwin G, Walker G, Westwood P, Marrs J, Thomson F, Cowley P, Christopoulos A, Pertwee RG, Ross RA (November 2005). "Allosteric modulation of the cannabinoid CB1 receptor". Molecular Pharmacology 68 (5): 1484–95. doi:10.1124/mol.105.016162. PMID 16113085.