Ro 04-6790

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Ro 04-6790
Ro04-6790 structure.png
Systematic (IUPAC) name
4-amino-N-[2,6-bis(methylamino)-4-pyrimidinyl]-benzenesulfonamide
Identifiers
CAS Number 202466-68-0
ATC code none
PubChem CID: 5312145
IUPHAR/BPS 274
ChemSpider 4471575
ChEMBL CHEMBL433461
Chemical data
Formula C12H16N6O2S
Molecular mass 308.359 g/mol
  • Nc2ccc(cc2)S(=O)(=O)Nc1cc(NC)nc(NC)n1
  • InChI=1S/C12H16N6O2S/c1-14-10-7-11(17-12(15-2)16-10)18-21(19,20)9-5-3-8(13)4-6-9/h3-7H,13H2,1-2H3,(H3,14,15,16,17,18)
  • Key:JELFWSXQTXRMAJ-UHFFFAOYSA-N
  (verify)

Ro 04-6790 is a drug, developed by Hoffmann–La Roche, which has applications in scientific research. It acts as a potent and selective receptor antagonist for the 5-HT6 serotonin receptor subtype, with little or no affinity at other receptors. In common with other drugs of this class,[1] Ro 04-6790 has nootropic effects in animals,[2] and reduces the amnesia produced by memory-impairing drugs such as dizocilpine[3] and scopolamine.[4]

References

  1. ↑ Fone KC. An update on the role of the 5-hydroxytryptamine6 receptor in cognitive function. Neuropharmacology. 2008 Nov;55(6):1015-22. doi:10.1016/j.neuropharm.2008.06.061 PMID 18655798
  2. ↑ King MV, Spicer CH, Sleight AJ, Marsden CA, Fone KC. Impact of regional 5-HT depletion on the cognitive enhancing effects of a typical 5-ht(6) receptor antagonist, Ro 04-6790, in the Novel Object Discrimination task. Psychopharmacology (Berlin). 2008 Oct 7. PMID 18839151
  3. ↑ Pitsikas N, Zisopoulou S, Pappas I, Sakellaridis N. The selective 5-HT(6) receptor antagonist Ro 04-6790 attenuates psychotomimetic effects of the NMDA receptor antagonist MK-801. Behavioural Brain Research. 2008 Apr 9;188(2):304-9. PMID 18164078
  4. ↑ Woolley ML, Marsden CA, Sleight AJ, Fone KC. Reversal of a cholinergic-induced deficit in a rodent model of recognition memory by the selective 5-HT6 receptor antagonist, Ro 04-6790. Psychopharmacology (Berlin). 2003 Dec;170(4):358-67. PMID 13680084



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