Pentiapine
CAS No. 81382-51-6
Pentiapine ( CGS 10746 )
产品货号. M26364 CAS No. 81382-51-6
喷硫平是一种新型多巴胺释放抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥8060 | 有现货 |
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| 10MG | ¥12879 | 有现货 |
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| 25MG | ¥19035 | 有现货 |
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| 50MG | ¥25758 | 有现货 |
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| 100MG | ¥34749 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Pentiapine
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述喷硫平是一种新型多巴胺释放抑制剂。
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产品描述Pentiapine is a novel inhibitor of dopamine release. (In Vivo):Pentiapine dose-dependently reduces motor activity of mice. Pentiapine dose-dependently reduces morphine-induced hyperactivity. Newman-Keuls post-hoc comparisons indicate that the group receiving morphine plus saline presents more activity than the groups receiving morphine plus 2 (P<0.05), 4, 8, 16, 24 and 32 (P<0.01) mg/kg of Pentiapine. Moreover, the groups receiving morphine plus 0.5, 1 and 2 mg/kg of Pentiapine present more activity than the groups receiving morphine plus 4, 8, 16, 24 and 32 mg/kg of Pentiapine (P<0.01). 30 mg/kg dose of Pentiapine completely blocks the methylenedioxymethamphetamine (MDMA) conditioned place preference (CPP) and also blocks the establishment of a cocaine CPP.
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体外实验——
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体内实验Pentiapine is a novel dopamine release inhibitor.The results show that Pentiapine dose-dependently reduces motor activity of mice. Moreover, Pentiapine dose-dependently reduces morphine-induced hyperactivity. Newman-Keuls post-hoc comparisons indicate that the group receiving morphine plus saline presents more activity than the groups receiving morphine plus 2 (P<0.05), 4, 8, 16, 24 and 32 (P<0.01) mg/kg of Pentiapine. Moreover, the groups receiving morphine plus 0.5, 1 and 2 mg/kg of Pentiapine present more activity than the groups receiving morphine plus 4, 8, 16, 24 and 32 mg/kg of Pentiapine (P<0.01). 30 mg/kg dose of Pentiapine completely blocks the methylenedioxymethamphetamine (MDMA) conditioned place preference (CPP) and also blocks the establishment of a cocaine CPP.
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同义词CGS 10746
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体H1 receptor| H2 receptor
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研究领域——
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适应症——
化学信息
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CAS Number81382-51-6
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分子量299.4
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分子式C15H17N5S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 100 mg/mL (334.01 mM)
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SMILESCN1CCN(CC1)C1=Nc2ccccc2Sc2nccn12
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Tripathi T, Shahid M, Khan HM, Negi MP, Siddiqui M, Khan RA. Modulation of in vivo immunoglobulin production by endogenous histamine and H1R and H2R agonists and antagonists. Pharmacol Rep. 2010 Sep-Oct;62(5):917-25.
产品手册
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