
A-437203
CAS No. 220519-06-2
A-437203 ( —— )
产品货号. M32764 CAS No. 220519-06-2
A-437203 是一种选择性的 D3 受体拮抗剂, 作用于 D2, D3, 和 D4 受体, Ki 值分别为 71, 1.6 和 6220 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥1951 | 有现货 |
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5MG | ¥2818 | 有现货 |
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10MG | ¥3957 | 有现货 |
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25MG | ¥5959 | 有现货 |
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50MG | ¥7718 | 有现货 |
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100MG | ¥10481 | 有现货 |
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500MG | ¥21191 | 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A-437203
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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A-437203 是一种选择性的 D3 受体拮抗剂, 作用于 D2, D3, 和 D4 受体, Ki 值分别为 71, 1.6 和 6220 nM。
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产品描述A-437203 is a selective D3 receptor antagonist with Ki of 71, 1.6, and 6220 nM for D2, D3, and D4 receptors, respectively.
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体外实验A-437203 is an antagonist with high affinity for D3 receptors and relatively high selectivity compared to other dopamine receptor subtypes (44-fold selective for D3 vs D2).
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体内实验A-437203, a selective D3 receptor antagonist, is initially tested alone in rat forced swim test (FST). Doses of A-437203 evaluated are 0.52, 1.75, 5.24, and 17.46 μmol/kg i.p. Doses are chosen based on the selectivity of A-437203 for D3 vs D2 dopamine receptors and reports indicating that the effects of A-437203 at doses of 17.46 μmol/kg (10 mg/kg) or lower are clearly mediated by D3 but not D2 receptors, since higher doses of the compound such as 174.6 μmol/kg (100 mg/kg) are necessary to bind and block D2 receptor from the irreversible inactivation induced by the alkylating agent EEDG. ANOVA revealed no significant difference between the treatments for any of the behaviors analyzed (F4, 45=1.12, p=0.359 for immobility, F4, 45=0.188, p=0.943 for climbing, and F4, 45=1.634, p=0.182 for swimming). Based on these results, the dose of 17.46 μmol/kg i.p. of A-437203 is selected for further experiments.
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同义词——
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通路GPCR/G Protein
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靶点Dopamine Receptor
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受体Dopamine 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 Number220519-06-2
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分子量456.53
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分子式C20H27F3N6OS
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纯度>98% (HPLC)
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溶解度——
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SMILESC(F)(F)(F)C1=CC(=NC(C(C)(C)C)=N1)N2CCN(CCCSC=3NC(=O)C=CN3)CC2
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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. Basso AM, et al. Antidepressant-like effect of D(2/3) receptor-, but not D(4) receptor-activation in the rat forced swim test. Neuropsychopharmacology. 2005 Jul;30(7):1257-68.?
产品手册




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