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E-6801

From Wikipedia, the free encyclopedia
E-6801
Names
Preferred IUPAC name
6-Chloro-N-{3-[2-(dimethylamino)ethyl]-1H-indol-5-yl}imidazo[2,1-b][1,3]thiazole-5-sulfonamide
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C17H18ClN5O2S2/c1-22(2)6-5-11-10-19-14-4-3-12(9-13(11)14)21-27(24,25)16-15(18)20-17-23(16)7-8-26-17/h3-4,7-10,19,21H,5-6H2,1-2H3
    Key: RZAXUKVIIWUIOM-UHFFFAOYSA-N
  • CN(C)CCC1=CNC2=C1C=C(C=C2)NS(=O)(=O)C3=C(N=C4N3C=CS4)Cl
Properties
C17H18ClN5O2S2
Molar mass423.94 g mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

E-6801 is apartial agonist of the5-HT6 receptor.[1] It enhanced recognition memory and reversed the memory deficits ofscopolamine in an object recognition task in a rat model.[2] The mechanism of memory enhancement is due to a combined modulation ofcholinergic andglutamatergic neurotransmission.

See also

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References

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  1. ^Romero, G. (August 2006)."Efficacy of selective 5-HT6 receptor ligands determined by monitoring 5-HT6 receptor-mediated cAMP signaling pathways".British Journal of Pharmacology.148 (8):1133–43.doi:10.1038/sj.bjp.0706827.PMC 1752021.PMID 16865095.
  2. ^Kendall, I. (February 2011). "E-6801, a 5-HT6 receptor agonist, improves recognition memory by combined modulation of cholinergic and glutamatergic neurotransmission in the rat".Psychopharmacology.213 (2–3):413–30.doi:10.1007/s00213-010-1854-3.PMID 20405281.S2CID 10116984.
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Tryptamines
N-Acetyltryptamines
α-Alkyltryptamines
Triptans
Cyclized tryptamines
Isotryptamines
Related compounds
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