Aripiprazole (Synonyms: 阿立哌唑; OPC-14597)
目录号: PL12255 纯度: ≥99%
Aripiprazole (OPC-14597) 是一种非典型抗精神病药,是一种有效、高亲和力的多巴胺 D2 受体部分激动剂。Aripiprazole 在 5-HT2B 和 5-HT2A 受体上是一种反向激动剂,并在 5-HT1A、5-HT2C、D3 和 D4 受体上显示部分激动剂作用。Aripiprazole 可用于精神分裂症和 COVID19 的研究。
CAS No. :129722-12-9
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中文名称
Aripiprazole
中文别名
阿立哌唑;阿立哌啶;阿立哌唑晶型I,晶型II,晶型A(水合物),晶型B,晶型C,晶型D,晶型E,晶型F;阿立哌唑晶型II;阿立哌唑晶型C;阿立哌唑 EP标准品;阿立哌唑 USP标准品;阿立哌唑 标准品;阿立派唑 标准品;阿利哌唑;六氢吡啶并[4,3-d]嘧啶-2,4-(1H,3H)-二酮丙酸;曲马朵N-氧化物;7-[4-[4-(2, 3-二氯苯基)-1-哌嗪基]丁氧基]-3, 4-二氢-2(1H)-喹啉酮;阿立哌嗪;阿立哌唑晶型;阿立哌唑晶型B;阿立哌唑晶型 I;阿立哌唑D8;阿立哌唑原料A
英文名称
Aripiprazole
英文别名
7-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy]-3,4-dihydrocarbostyril;ABILIFY;ABILITAT;ARIPIPRAZOLE;OPC 14597;OPC 31;7-[4-[4-(2,3-dichlorophenyl)-1-piperazinyl]butoxy]-3,4-dihydro-2(1H)-quinolinone;OPC-14597, OPC-31,;7-[4-[4-(2,3-dichlorophenyl)piperazin-1-yl]butoxy]-3,4-dihydro-1H-quinolin-2-one;Arpiprazole;Alipiprazole;7-[4-[4-(2,3-Dichlorophenyl)-1-piperazinyl-d8]butoxy]-3,4-dihydro-2(1H)-quinolinone;7-[4-[4-(2,3-Dichlorophenyl)-1-piperazinyl-d8]butoxy]-3,4-dihydrocarbostyril;Abilify-d8;Abilitat-d8;OPC 14597-d8;Aripiprazole (OPC-14597,Abilify®, Aripiprex®);Aripiprazole solution;7-{4-[4-(2,3-Dichlorophenyl)-1-piperazinyl]butoxy}-3,4-dihydro-2(1H)-quinolinone;Aripirazole;OPC 31-d8-;OPC-14597;Aripiprazole;7-[4-[4-(2,3-Dichlorophenyl)-1-piperazinyl]butoxy]-3,4-dihydro-2(1H)-quinolinone
Cas No.
129722-12-9
分子式
C23H27Cl2N3O2
分子量
448.39
包装储存
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
产品详情
Aripiprazole (OPC-14597) 是一种非典型抗精神病药,是一种有效、高亲和力的多巴胺 D2 受体部分激动剂。Aripiprazole 在 5-HT2B 和 5-HT2A 受体上是一种反向激动剂,并在 5-HT1A、5-HT2C、D3 和 D4 受体上显示部分激动剂作用。Aripiprazole 可用于精神分裂症和 COVID19 的研究。
生物活性
Aripiprazole (OPC-14597), an atypical antipsychotic, is a potent and high-affinity dopamine D2 receptor partial agonist. Aripiprazole is an inverse agonist at 5-HT2B and 5-HT2A receptors and displays partial agonist actions at 5-HT1A, 5-HT2C, D3, and D4 receptors. Aripiprazole can be used for the research of schizophrenia and COVID19.
性状
Solid
IC50 & Target[1][2]
5-HT1A Receptor 4.2 nM (Ki) 5-HT2A Receptor
体外研究(In Vitro)
Aripiprazole potently activates D2 receptor-mediated inhibition of cAMP accumulation.
Aripiprazole shows a greater anti-inflammatory effect on TNF-α, IL-13, IL-17α and fractalkine. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Aripiprazole (0-3 mg/kg, IP, daily) shows some anxiolytic properties. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: WAG/Rij rats (N = 6 per dose, 6 months, administration of a mixtu
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, protect from light In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)
ClinicalTrial
参考文献
[1]. Burris KD, et al. Aripiprazole, a novel antipsychotic, is a high-affinity partial agonist at human dopamine D2 receptors. J Pharmacol Exp Ther. 2002 Jul;302(1):381-9.
[2]. Davies MA, et al. Aripiprazole: a novel atypical antipsychotic drug with a uniquely robust pharmacology. CNS Drug Rev. 2004 Winter;10(4):317-36.
溶解度数据
In Vitro: DMSO : 100 mg/mL (223.02 mM; Need ultrasonic)DMF : 50 mg/mL (111.51 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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