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AGH-192

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
AGH-192
Identifiers
  • 3-(3-ethylimidazol-4-yl)-4-fluoro-5-iodo-1H-indole
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC13H11FIN3
Molar mass355.155 g·mol−1
3D model (JSmol)
  • CCN1C=NC=C1C2=CNC3=C2C(=C(C=C3)I)F
  • InChI=1S/C13H11FIN3/c1-2-18-7-16-6-11(18)8-5-17-10-4-3-9(15)13(14)12(8)10/h3-7,17H,2H2,1H3
  • Key:KBQLQDPQEMFGCB-UHFFFAOYSA-N

AGH-192 is a potent and selective, water soluble, orally bioavailable and brain penetrant fullagonist at the5-HT7serotoninreceptor of theimidazolylindole family, derived from the older drugAGH-107. In animal tests it showed activity indicative of potential application in the treatment ofneuropathic pain.[1]

See also

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References

[edit]
  1. ^Hogendorf AS, Hogendorf A, Popiolek-Barczyk K, Ciechanowska A, Mika J, Satała G, Walczak M, Latacz G, Handzlik J, Kieć-Kononowicz K, Ponimaskin E, Schade S, Zeug A, Bijata M, Kubicki M, Kurczab R, Lenda T, Staroń J, Kurczab R, Satała G, Lenda T, Walczak M, Latacz G, Handzlik J, Kieć-Kononowicz K, Wierońska JM, Woźniak M, Cieślik P, Bugno R, Staroń J, Bugno R, Duszyńska B, Pilarski B, Bojarski AJ (2019). "Fluorinated indole-imidazole conjugates: Selective orally bioavailable 5-HT7 receptor low-basicity agonists, potential neuropathic painkillers".European Journal of Medicinal Chemistry.170:261–275.doi:10.1016/j.ejmech.2019.03.017.PMID 30904783.S2CID 85498356.
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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