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210688-56-5

210688-56-5 Structure

210688-56-5 Structure
IdentificationBack Directory
[Name]

3-[2-[4-(3,4-dimethylphenyl)-1-piperazinyl]ethyl]-2,3-dihydro-1H-isoindol-1-onedihydrochloride
[CAS]

210688-56-5
[Synonyms]

PD 168568 dihydrochl
PD 168568 dihydrochloride
1H-Isoindol-1-one, 3-[2-[4-(3,4-dimethylphenyl)-1-piperazinyl]ethyl]-2,3-dihydro-
3-[2-[4-(3,4-dimethylphenyl)-1-piperazinyl]ethyl]-2,3-dihydro-1H-isoindol-1-onedihydrochloride
[Molecular Formula]

C22H27N3O
[MDL Number]

MFCD12828776
[MOL File]

210688-56-5.mol
[Molecular Weight]

349.47
Chemical PropertiesBack Directory
[storage temp. ]

Desiccate at RT
[solubility ]

Soluble to 50 mM in water and to 100 mM in DMSO
[form ]

Powder
Hazard InformationBack Directory
[Uses]

PD 168568 is a selective D4 receptor affinity.
[in vivo]

PD 168568 (3 mg/kg, Oral) has ability to inhibit amphetamine-stimulated locomotor activity in the rat[3].

Animal Model:Rat[1]
Dosage:3 mg/kg
Administration:Oral administration
Result:Inhibited amphetamine (0.5 mg/kg, i.p.) stimulated locomotor activity.
[IC 50]

D4 Receptor: 8.8 nM (Ki); D2 Receptor: 1842 nM (Ki); D3 Receptor: 2682 nM (Ki)
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