Ro4938581

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Ro4938581
Ro4938581.svg
Systematic (IUPAC) name
3-bromo-10-(difluoromethyl)-9H-benzo[f]imidazo[1,5-a][1,2,4]triazolo[1,5-d][1,4]diazepine
Identifiers
PubChem CID: 11624499
IUPHAR/BPS 4299
ChemSpider 9799246
ChEMBL CHEMBL1080588
Chemical data
Formula C13H8BrF2N5
Molecular mass 352.14 g/mol
  • FC(F)C(N=C1)=C(N1C2=C3C=C(Br)C=C2)CN4C3=NC=N4
  • InChI=1S/C13H8BrF2N5/c14-7-1-2-9-8(3-7)13-17-5-19-21(13)4-10-11(12(15)16)18-6-20(9)10/h1-3,5-6,12H,4H2
  • Key:AFJRYPJIKHMNGL-UHFFFAOYSA-N

Ro4938581 is a nootropic drug invented in 2009 by a team working for Hoffmann-La Roche, which acts as a subtype-selective inverse agonist at the α5 subtype of the benzodiazepine binding site on the GABAA receptor. It has good selectivity for the α5 subtype and did not produce convulsant or anxiogenic effects in animal studies, making it a promising potential nootropic.[1][2][3] Ro4938581 and a related derivative basmisanil (RG-1662, RO5186582) have subsequently been investigated for the alleviation of cognitive dysfunction in Down syndrome.[4][5]

See also

References

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  5. Inhibiting Inhibition to Treat Down Syndrome Symptoms

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