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Merck

F4429

Sigma-Aldrich

FAUC 213

≥98% (HPLC), solid

Synonym(e):

2-[4-(4-Chlorophenyl)piperazin-1-ylmethyl]pyrazolo[1,5-a]pyridine

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About This Item

Empirische Formel (Hill-System):
C18H19ClN4
CAS-Nummer:
Molekulargewicht:
326.82
MDL-Nummer:
UNSPSC-Code:
12352200
PubChem Substanz-ID:
NACRES:
NA.77

Assay

≥98% (HPLC)

Form

solid

Farbe

white

Löslichkeit

DMSO: ~24 mg/mL (with warming up to 60 °C)
H2O: insoluble

Lagertemp.

2-8°C

SMILES String

Clc1ccc(cc1)N2CCN(CC2)Cc3cc4ccccn4n3

InChI

1S/C18H19ClN4/c19-15-4-6-17(7-5-15)22-11-9-21(10-12-22)14-16-13-18-3-1-2-8-23(18)20-16/h1-8,13H,9-12,14H2

InChIKey

DTRXURJDKOYCCD-UHFFFAOYSA-N

Angaben zum Gen

Anwendung

FAUC 213 has been used as a selective dopamine receptor D4-R antagonist:
  • to test its effect on the expression of luteinizing hormone in eel pituitary primary cell culture
  • to test its effect on bupropion induced hypophagia and locomotion in rats
  • to test its modulatory effects on rat basolateral amygdala in the presence of dopamine

Biochem./physiol. Wirkung

FAUC 213 displays antipsychotic properties and may be of use in studies related to behavioral neurobiology and neurochemistry.
Highly selective D4 dopamine receptor full antagonist

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Die Dokumentenbibliothek aufrufen

S Löber et al.
Journal of medicinal chemistry, 44(17), 2691-2694 (2001-08-10)
Structure dependent efficacy studies in the field of selective D4 ligands led to the 2-aminomethyl substituted azaindole 2 (FAUC 213) that displayed strong D4 binding, high subtype selectivity, and complete antagonist properties in ligand-induced mitogenesis experiments. According to our schematic
Frank Boeckler et al.
Psychopharmacology, 175(1), 7-17 (2004-03-10)
2-[4-(4-Chlorophenyl)piperazin-1-ylmethyl]pyrazolo[1,5-a]pyridine (FAUC 213) is a highly selective antagonist at the dopamine D(4) receptor subtype. It was designed as a derivative of two partial antagonists and has been proven to be a complete antagonist in mitogenesis assay. In the present study
Blocking alpha2A adrenoceptors, but not dopamine receptors, augments bupropion-induced hypophagia in rats.
Janhunen, et al.
Obesity (Silver Spring, Md.), 21, E700-E708 (2017)
Hironori Ohshiro et al.
Neuropharmacology, 61(4), 857-866 (2011-06-21)
The amygdala receives dopaminergic innervation, and dopamine (DA) enhances various activities in cognitive and emotional behaviors. Periodic bursts of spontaneous inhibitory postsynaptic currents (IPSCs) with a low (<1 Hz) inter-event frequency have been observed in projection neurons of the basolateral
C Jolly et al.
Journal of neuroendocrinology, 28(9) (2016-07-28)
In various vertebrate species, dopamine (DA) exerts an inhibitory action on reproduction. In the European eel, DA plays a pivotal role in the inhibitory control of gonadotroph function and the blockade of puberty. In vivo studies have suggested that this

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