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AGH-107

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
AGH-107
Clinical data
ATC code
  • None
Identifiers
  • 3-(3-ethylimidazol-4-yl)-5-iodo-1H-indole
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H12IN3
Molar mass337.164 g·mol−1
3D model (JSmol)
  • CCn1cncc1-c1c[nH]c2ccc(I)cc12
  • InChI=1S/C13H12IN3/c1-2-17-8-15-7-13(17)11-6-16-12-4-3-9(14)5-10(11)12/h3-8,16H,2H2,1H3
  • Key:JLCILCCDUVFIRF-UHFFFAOYSA-N

AGH-107 is a potent, selective, water-soluble and brain penetrant fullagonist at the5-HT7serotoninreceptor of theimidazolylindole family.[1] AGH-107 is one of the few examples of low-basicity aminergic receptor agonists, which may underlie its high selectivity over the related central nervous system targets. AGH-107 was found to reverse the impairment in novel object recognition caused byMK-801 inmice. The relatively short half-life inrodents inhibited its use as amolecular probe.

See also

[edit]

References

[edit]
  1. ^Hogendorf AS, Hogendorf A, Kurczab R, Satała G, Lenda T, Walczak M, et al. (May 2017)."7 Receptor Agonists Synthesized Using the van Leusen Multicomponent Protocol".Scientific Reports.7 (1): 1444.doi:10.1038/s41598-017-00822-4.PMC 5431432.PMID 28473721.
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
4-Hydroxytryptamines
andesters/ethers
5-Hydroxy- and
5-methoxytryptamines
N-Acetyltryptamines
α-Alkyltryptamines
α-Ketotryptamines
Cyclized tryptamines
Isotryptamines
Related compounds
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