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VU-0238429
1-(4-methoxybenzyl)-5-(trifluoromethoxy)indole-2,3-dione
PubChem CID ChemSpider ChEMBL CompTox Dashboard (EPA ) Formula C 17 H 12 F 3 N O 4 Molar mass 351.276 g/mol g·mol−1 3D model (JSmol )
c2cc(OC)ccc2CN(C(=O)C1=O)c3ccc(cc13)OC(F)(F)F
COc1ccc(cc1)CN2c3ccc(cc3C(=O)C2=O)OC(F)(F)F
InChI=1S/C17H12F3NO4/c1-24-11-4-2-10(3-5-11)9-21-14-7-6-12(25-17(18,19)20)8-13(14)15(22)16(21)23/h2-8H,9H2,1H3
Y Key:CKLGZXFOLMHCMC-UHFFFAOYSA-N
Y
(verify)
VU-0238429 is a drug which acts as a selective positive allosteric modulator for the muscarinic acetylcholine receptor M5 . It was the first selective ligand developed for the M5 subtype,[ 1] and is structurally derived from older M1 -selective positive allosteric modulators such as VU-0119498.[ 2] [ 3] Replacing the O -methyl- by a phenylgroup further improves the receptor subtype selectivity (VU-0400265 ).
References
^ Bridges TM, Marlo JE, Niswender CM, et al. (June 2009). "Discovery of the first highly M5-preferring muscarinic acetylcholine receptor ligand, an M5 positive allosteric modulator derived from a series of 5-trifluoromethoxy N-benzyl isatins" . Journal of Medicinal Chemistry . 52 (11): 3445–8. doi :10.1021/jm900286j . PMC 3875304 . PMID 19438238 .
^ Conn PJ, Jones CK, Lindsley CW (March 2009). "Subtype-selective allosteric modulators of muscarinic receptors for the treatment of CNS disorders" . Trends in Pharmacological Sciences . 30 (3): 148–55. doi :10.1016/j.tips.2008.12.002 . PMC 2907736 . PMID 19201489 .
^ Bridges, T. M.; Kennedy, J. P.; Hopkins, C. R.; Conn, P. J.; Lindsley, C. W. (2010). "Heterobiaryl and heterobiaryl ether derived M5 positive allosteric modulators" . Bioorganic & Medicinal Chemistry Letters . 20 (19): 5617. doi :10.1016/j.bmcl.2010.08.042 . PMC 3179183 . PMID 20801651 .
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