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Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.
Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
25 mg | ¥ 10,600 | 6-8周 | |
50 mg | ¥ 13,800 | 6-8周 | |
100 mg | ¥ 17,500 | 6-8周 |
Bifeprunox 相关产品
产品描述 | Bifeprunox is a potent partial agonist of dopamine D2-like and 5-HT1A receptor (pEC50: 6.37 for hippocampus 5-HT1A; pKis: 7.19 and 8.83 for cortex 5-HT1A and striatum D2). It is an antipsychotic for the research of schizophrenia. |
靶点活性 | 5-HT1A receptor:7.19 (pKi), 5-HT1A receptor:6.37(pEC50), D2 receptor:8.83 (pKi) |
体外活性 | Bifeprunox has a pKi of 8 at h5-HT1A receptors (Emax: 70%) [1]. |
体内活性 | Bifeprunox (0.001-2.5 mg/kg) reduces marble burying in mice [2]. Bifeprunox (4-250 μg/kg) influences nicotine-seeking behavior in response to drug-associated stimuli in rats [3]. |
分子量 | 385.46 |
分子式 | C24H23N3O2 |
CAS No. | 350992-10-8 |
密度 | 1.247g/cm3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。
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