ChemicalBook--->CAS DataBase List--->669770-29-0

669770-29-0

669770-29-0 Structure

669770-29-0 Structure
IdentificationBack Directory
[Name]

AQW-051
[CAS]

669770-29-0
[Synonyms]

AQW-051
669770-29-0
AQW-051 (AQW051
(R)-3-((6-(p-Tolyl)pyridin-3-yl)oxy)quinuclidine
1-Azabicyclo[2.2.2]octane, 3-[[6-(4-methylphenyl)-3-pyridinyl]oxy]-, (3R)-
[Molecular Formula]

C19H22N2O
[MDL Number]

MFCD28502153
[MOL File]

669770-29-0.mol
[Molecular Weight]

294.39
Chemical PropertiesBack Directory
[Boiling point ]

443.8±45.0 °C(Predicted)
[density ]

1.18±0.1 g/cm3(Predicted)
[storage temp. ]

Store at 0-8 °C
[solubility ]

Ethanol: Soluble: =10 mg/ml
[form ]

Solid
[pka]

9.09±0.33(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313
Hazard InformationBack Directory
[Uses]

VQW-765 (AQW-051) is a selective and orally active alpha-7 nicotinic acetylcholine receptor (α7-nAChR) agonist with a pKD value of 7.56 to recombinantly expressed human α7-nAChR. VQW-765 shows anxiolytic-like effect in vivo. VQW-765 can be used for the research of anxiety disorder and acute performance anxiety[1].
[in vivo]

VQW-765 (0.03 and 0.3 mg/kg; oral administration once) increases cognitive effect and learning/memory performance in mice[1]. VQW-765 (1 mg/kg; oral administration once) shows anxiolytic-like effect with increasing the social exploration time in rats with a duration of at least 6 h[1].

Animal Model:OF1/IC strain adult mice[1]
Dosage:0.03 and 0.3 mg/kg
Administration:Oral administration; 0.03 and 0.3 mg/kg once
Result:Increased the learning/memory performance with more time to scrutinize the novel partner than the familiar partner during the re-test trial at 24 h. Showed cognitive-enhancing effects in mice by the object recognition test (ORT).
[References]

[1] Feuerbach D, et al. AQW051, a novel, potent and selective α7 nicotinic ACh receptor partial agonist: pharmacological characterization and phase I evaluation. Br J Pharmacol. 2015 Mar;172(5):1292-304. DOI:10.1111/bph.13001
Spectrum DetailBack Directory
[Spectrum Detail]

AQW-051(669770-29-0)1HNMR
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