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6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide
Identifiers
  • 6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide
CAS Number
PubChemCID
ChemSpider
UNII
Chemical and physical data
FormulaC16H16ClN3O2
Molar mass317.77 g·mol−1
3D model (JSmol)
  • c3cccnc3NC(=O)N(c1cc2Cl)CCc1cc2OCC
  • InChI=1S/C16H16ClN3O2/c1-2-22-14-9-11-6-8-20(13(11)10-12(14)17)16(21)19-15-5-3-4-7-18-15/h3-5,7,9-10H,2,6,8H2,1H3,(H,18,19,21)
  • Key:OCFLVVOXCVJFTI-UHFFFAOYSA-N

6-Chloro-5-ethoxy-N-(pyridin-2-yl)indoline-1-carboxamide (CEPC) is a drug which acts as a potent and selectiveantagonist for theserotonin5-HT2Creceptor. In animal studies it was found to potentiate theconditioned place preference induced by low-doseamphetamine, demonstrating that 5-HT2C-mediated disinhibition of dopamine release can cause interactions with dopaminergic drugs.[1]

See also

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References

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  1. ^McCorvy JD, Harland AA, Maglathlin R, Nichols DE (November 2011)."A 5-HT(2C) receptor antagonist potentiates a low dose amphetamine-induced conditioned place preference".Neuroscience Letters.505 (1):10–3.doi:10.1016/j.neulet.2011.07.036.PMC 3213641.PMID 21827831.
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
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