Edge Rewrite
// HTMLRewriter · presentation

This page was redesigned at the edge.

Cloudflare fetched the original article and streamed it through HTMLRewriter to apply an entirely new visual system without rebuilding the source page.

Jump to content

AHR-1229

From Wikipedia, the free encyclopedia
AHR-1229
Clinical data
Other namesAHR1229; N-Butyl-N-(1-phenylpyrrolidin-4-yl)tryptamine; 3-[2-(3-Indolyl-)ethyl]butylamino-1-phenylpyrrolidine
ATC code
  • None
Identifiers
  • N-butyl-N-[2-(1H-indol-3-yl)ethyl]-1-phenylpyrrolidin-3-amine
PubChem CID
ChemSpider
Chemical and physical data
FormulaC24H31N3
Molar mass361.533 g·mol−1
3D model (JSmol)
  • CCCCN(CCC1=CNC2=CC=CC=C21)C3CCN(C3)C4=CC=CC=C4
  • InChI=1S/C24H31N3/c1-2-3-15-26(16-13-20-18-25-24-12-8-7-11-23(20)24)22-14-17-27(19-22)21-9-5-4-6-10-21/h4-12,18,22,25H,2-3,13-17,19H2,1H3
  • Key:CDYYGETYBLUMPO-UHFFFAOYSA-N

AHR-1229, also known as N-butyl-N-(1-phenylpyrrolidin-4-yl)tryptamine, is a drug of the tryptamine family which was studied as a possible dopamine antagonist.[1] It increases alertness and produces "small repetitive head movements" in rodents, effects said to be indicative of behavioral excitation, whereas it modestly antagonizes intra-accumbens dopamine-induced hyperlocomotion.[1] Conversely, the drug did not produce catalepsy, did not affect amphetamine-induced lethality, did not affect prolactin levels, and did not displace spiperone binding to dopamine receptors.[1] AHR-1229 was first described in the scientific literature by 1983.[1]

See also

[edit]

References

[edit]
  1. 1 2 3 4 Costall B, Dannenburg WN, Johnson DN, Naylor RJ (April 1983). "Aminoalkylindoles: atypical dopamine antagonists". J Pharm Pharmacol. 35 (4): 229–233. doi:10.1111/j.2042-7158.1983.tb02918.x. PMID 6133932.