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- CAS号:
67165-56-4
- 规格:
5mg/10mg/25mg/50mg/100mg
| 规格: | 5mg | 产品价格: | ¥373.0 |
|---|---|---|---|
| 规格: | 10mg | 产品价格: | ¥636.0 |
| 规格: | 25mg | 产品价格: | ¥1144.0 |
| 规格: | 50mg | 产品价格: | ¥1716.0 |
| 规格: | 100mg | 产品价格: | ¥2575.0 |
Product Introduction
Bioactivity
| 名称 | Diclofensine |
| 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). |
| 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]. |
| 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]。 |
| 存储条件 | Keep away from direct sunlight,Store at low temperature Pure form: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 关键字 | SLC6A3 | Neuroscience | MonoamineTransporter | Monoamine transporter | DopamineReceptor | Dopamine Transporter | Dopamine Receptor | Dopamine | Diclofensine | DAT | 5HTReceptor | 5HT Receptor | 5-HT |
| 相关产品 | Cefaclor monohydrate | Hexamethonium Bromide | Cinchonidine | Oxolinic acid | Alverine citrate | Dapoxetine hydrochloride | L-DOPA | Mianserin hydrochloride | Trazodone hydrochloride | 1,8-Cineole | Octopamine hydrochloride | Creatine |
| 相关库 | Inhibitor Library | CNS-Penetrant Compound Library | Angiogenesis related Compound Library | Bioactive Compound Library | Anti-Cancer Compound Library | Bioactive Compounds Library Max | ReFRAME Related Library | Neurotransmitter Receptor Compound Library | Neuronal Signaling Compound Library | Serotonin Receptor-Targeted Compound Library | GPCR Compound Library | Membrane Protein-targeted Compound Library |
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荷,而与其相联的氮原子则带负电荷,因而“头部”有极性,是亲水的。另外还有一个含羰基的同素环(含相同元素的环),其上一个羧基以酯键与甲醇相结合。环D上有一个丙酸侧链以酯键与叶绿醇相结合,叶绿醇是由四个异戊二烯单位所组成的双萜,是亲脂的,能伸入类囊体的拟脂层,故叶绿素能定向排列。卟环上的共轭双键和中央镁原子容易被光激发而引起电子的得失,这决定了叶绿素具有特殊的光化学性质。 卟啉环中的镁可被H+、Cu2+、Zn2+ 等所置换。当为H+所置换后,即形成褐色的去镁叶绿素(pheophytin,Pheo)。去镁叶绿素
的0.2%。它们表达CD56,NKG2D,CD28,HLA-DR,CD161和T细胞活化标志物CD69,但不表达CD25,NKG2A或NKG2C。Vδ3T细胞在肝脏和肠道中是丰富的,并且参与慢性病毒感染和白血病。扩增的Vδ3T细胞仅识别CD1d并释放Th1,Th2和Th17细胞因子以诱导树突状细胞成熟成APC。它们不识别 CD1a、CD1b 或 CD1c 。Vδ3 T细胞和B细胞相互调节成熟标志物CD40,CD86和HLA-DR的表达,并促进B细胞的IgM释放。 此外,在淋巴瘤患者的PB中观察到Vδ
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