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(+)-PD 128907 hydrochloride

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Chemical Structure| 300576-59-4 同义名 : -
CAS号 : 300576-59-4
货号 : A156825
分子式 : C14H20ClNO3
纯度 : 98%
分子量 : 285.767
MDL号 : MFCD00210210
存储条件:

粉末 Keep in dark place,Inert atmosphere,Room temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 20 mg/mL(69.99 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 15 mg/mL(52.49 mM),配合低频超声助溶

动物实验配方:
生物活性
描述 The D3 receptor is thought to play a role in reinforcement pathways because it is expressed in high levels within the mesolimbic dopaminergic system and, more specifically, the nucleus accumbens shell. (+)-PD 128907 HCl is a dopaminergic agonist with a range of in vitro D3 selectivity[1]. Low doses of (+)-PD 128907 reduced spontaneous locomotor activity in the rat (ED50 = 13 ± 3 μg/kg, s.c.) a response which was comparable with the non-selective D2,3 receptor agonist apomorphine (ED50 = 13 ± 1.6 μg/kg, s.c.). In addition, (+)-PD 128907 impaired prepulse inhibition of the acoustic startle response, with significant effects observed at doses of 30 μg/kg when appropriate prepulse intensities were used. Higher doses of (+)-PD 128907 HCl reversed gamma-butyrolactone-induced catecholamine synthesis (ED50 = 95 ± 22 and 207 ± 37 μg/kg in accumbens and striatum respectively) and induced yawning (100-300 μg/kg), penile grooming (30-1000 μg/kg) and sniffing (> or = 300 μg/kg). In addition, the observation that (+)-PD 128907 disrupts prepulse inhibition, a phenomenon which is also impaired in schizophrenic subjects[2].
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

3.50mL

0.70mL

0.35mL

17.50mL

3.50mL

1.75mL

34.99mL

7.00mL

3.50mL

参考文献

[1]Collins GT, Witkin JM, Newman AH, et al. Dopamine agonist-induced yawning in rats: a dopamine D3 receptor-mediated behavior. J Pharmacol Exp Ther. 2005;314(1):310‐319

[2]Bristow LJ, Cook GP, Gay JC, et al. The behavioural and neurochemical profile of the putative dopamine D3 receptor agonist, (+)-PD 128907, in the rat. Neuropharmacology. 1996;35(3):285‐294