PARDOPRUNOX.HCL

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更新时间： 2024-01-22 09:22:03

CAS号：269718-83-4

常用名： 盐酸Pardoprunox

价格：
￥需询单/1mg

纯度： 98.0%

备货期： 3天

库存： 现货

其他详情（用途，包装）：
用途： Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT1A receptor agonist, D2 (pKi = 8.1) and D3 receptor (pKi = 8.6) partial agonist and 5-HT1A receptor (pKi = 8.5) full agonist.IC50 value: 8.1/8.6/8.5 (pKi, for D2/ D3/5-HT1A receptor)Target: dopamine D2 and D3 receptor, 5-HT1A receptorin vitro: Pardoprunox also binds to D4 (pKi = 7.8), α1-adrenergic (pKi = 7.8), α2-adrenergic (pKi = 7.4), and 5-HT7 receptors (pKi = 7.2) with lower affinity. Pardoprunox acts as a potent but partial D(2) receptor agonist (pEC50 = 8.0 and pA2 = 8.4) with an efficacy of 50% on forskolin stimulated cAMP accumulation. At human recombinant dopamine D3 receptors, Pardoprunox acts as a partial agonist in the induction of [35S]GTPgammaS binding (intrinsic activity of 67%; pEC(50) = 9.2) and antagonized the dopamine induction of [35S]GTPgammaS binding (pA2 = 9.0). Pardoprunox acts as a full 5-HT1A receptor agonist on forskolin induced cAMP accumulation at cloned human 5-HT1A receptors but with low potency (pEC50 = 6.3) [1].in vivo: Pardoprunox induces contralateral turning behaviour in rats with unilateral 6-hydroxydopamine-induced lesions of the substantia nigra pars compacta (SNpc) (MED=0.03mg/kg; po). In MPTP-treated common marmosets, Pardoprunox dose-dependently increases locomotor activity (MED=0.03mg/kg; po) and decreases motor disability (MED=0.03mg/kg; po). In contrast Pardoprunox attenuated novelty-induced locomotor activity (MED=0.01mg/kg; po), (+)-amphetamine-induced hyperlocomotion (MED=0.3mg/kg; po) and apomorphine-induced climbing (MED=0.6mg/kg; po) in rodents. Pardoprunox also induces 5-HT1A receptor-mediated behaviours, including flat body posture and lower lip retraction (MED=0.3mg/kg; po). Collectively, these findings demonstrate that Pardoprunox possesses dopamine D2/3 partial agonist effects, 5-HT1A agonist effects and reduces parkinsonism in animal models. functional D2 receptor partial agonist activity and is effective in experimental models predictive of efficacy in PD.[2] 物理化学性质： CAS号：269718-83-4 常用中文名：盐酸Pardoprunox 常用英文名：Pardoprunox hydrochloride 分子式：C12H16ClN3O2 分子量：269.72700 密度：N/A 沸点：N/A 熔点：N/A 闪点：N/A 储存条件：2-8℃

供应商信息：

公司名：上海泽涵生物医药科技有限公司

认证状态： 未认证供应商

商品数： 1060件

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上海泽涵生物医药科技有限公司是集医药化学品（含中间体）、精细化学品和生物医药产品的研究、开发、生产、产品销售、技术服务于一体的高新企业。

其他供应商价格：

2022-11-29 价格：￥需询单 Pardoprunox.HCl(SLV-308)

2021-04-03 价格：￥7112.0 Pardoprunox (hydrochloride)

2024-03-12 价格：￥16999.9 盐酸帕多普诺（SLV-308）

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盐酸Pardoprunox价格

PARDOPRUNOX.HCL

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