化合物CGP 37849 T7720
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
100 mg | 127910-31-0 | ¥15,600.00 | 询底价 |
5 mg | 127910-31-0 | ¥3,880.00 | 询底价 |
25 mg | 127910-31-0 | ¥8,590.00 | 询底价 |
50 mg | 127910-31-0 | ¥11,500.00 | 询底价 |
1 mg | 127910-31-0 | ¥1,550.00 | 询底价 |
10 mg | 127910-31-0 | ¥5,580.00 | 询底价 |
Product Introduction
Bioactivity
英文名: CGP 37849
描述: CGP 37849 是一种竞争性口服活性 N-甲基-D-天冬氨酸 (NMDA) 受体拮抗剂((Ki = 35 nM)),具有有效性。CGP 37849 是啮齿动物的抗惊厥药,也具有抗抑郁和抗焦虑的特性。
体外活性: Within the hippocampal slice in vitro, CGP 37849 demonstrates reversible and selective antagonism against NMDA-induced increases in the firing rate of CA1 pyramidal cells. In the presence of a low Mg2+ level medium, concentrations of CGP 37849 up to 10 μM effectively inhibit burst firing evoked in CA1 neurons by stimulating Schaffer collateral-commissural fibers, while leaving the magnitude of the initial population spike unaffected.[1]
体内活性: In vivo, oral administration to rats of CGP 37849 selectively blocks firing in hippocampal neurons induced by ionophoretically-applied NMDA, without affecting the responses to quisqualate or kainate.[1] Oral administration to mice of CGP 37849 suppresses maximal electroshock-induced seizures in mice with an ED50 of 21 mg/kg.[1]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: H2O : 90.0 mg/mL (430.3 mM)
DMSO : Soluble
关键字: CGP 37849
相关产品: Orphenadrine hydrochloride | DNQX disodium salt | Ro 25-6981 | UBP551 | O-Phospho-L-serine | Procaine hydrochloride | DL-AP5 | Rapastinel Trifluoroacetate | Bupivacaine | Quininic acid
相关库: Anti-Neurodegenerative Disease Compound Library | Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Neuronal Signaling Compound Library | Bioactive Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途