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Diclofensine (Ro 8-4650) 是一种单胺再摄取抑制剂,在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。
Diclofensine (Ro 8-4650) 是一种单胺再摄取抑制剂,在大鼠脑突触体中能够阻断多巴胺 (IC50=0.74 nM)、去甲肾上腺素 (IC50=2.3 nM) 和 5-羟色胺 (IC50=3.7 nM)。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥ 467 | 6-8周 | |
10 mg | ¥ 795 | 6-8周 | |
25 mg | ¥ 1,431 | 6-8周 | |
50 mg | ¥ 2,146 | 6-8周 | |
100 mg | ¥ 3,219 | 6-8周 |
产品描述 | Diclofensine (Ro 8-4650) is a monoamine reuptake inhibitor that blocks dopamine (IC50=0.74 nM), norepinephrine (IC50=2.3 nM), and 5-hydroxytryptophan (IC50=3.7 nM) in synaptosomes of the rat brain. dAURK-4 hydrochloride is an inhibitor of dopamine (IC50=0.74 nM), norepinephrine (IC50=2.3 nM) and 5-hydroxytryptophan (IC50=3.7 nM). |
体内活性 | 在一项对抗抑郁症治疗中使用新型精神活性化合物 diclofensine的对照试验中[1]。 |
动物实验 | In a controlled study, out-patients suffering from moderate to severe depression were treated with the objective of assessing the new drug's therapeutically effective dose range. Maprotiline was used as a reference drug: fourteen patients were assigned to receive diclofensine and thirteen to receive maprotiline in a double-blind design. Depending on tolerance and efficacy, they were treated for periods ranging from 5 to 150 days. Doses were titrated to the optimum[1]. |
别名 | 双氮奋兴, Ro 8-4650 |
分子量 | 322.23 |
分子式 | C17H17Cl2NO |
CAS No. | 67165-56-4 |
Smiles | COc1ccc2C(CN(C)Cc2c1)c1ccc(Cl)c(Cl)c1 |
密度 | 1.242g/cm3 |
存储 | keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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