8-溴-cGMP钠 T14064
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 |
---|---|---|---|
25 mg | 51116-01-9 | ¥1,830.00 | 询底价 |
100 mg | 51116-01-9 | ¥4,350.00 | 询底价 |
1 mg | 51116-01-9 | ¥248.00 | 询底价 |
5 mg | 51116-01-9 | ¥578.00 | 询底价 |
50 mg | 51116-01-9 | ¥2,890.00 | 询底价 |
10 mg | 51116-01-9 | ¥913.00 | 询底价 |
Product Introduction
Bioactivity
英文名: 8-Bromo-cGMP sodium
描述: 8-Bromo-cGMP sodium 是一种 PKG 激活剂, 是 cGMP 的膜渗透性类似物。8-Bromo-cGMP sodium 具有缓解疼痛和血管舒张作用,可显着抑制 Ca2+ 宏观电流,抑制高 K+ 刺激的胰岛素释放。
体外活性: 8-Bromo-cGMP sodium (1 µM-0.1 mM) can inhibit acetylcholine-induced increases in intracellular calcium concentrations.[1]8-Bromo-cGMP sodium (1-100 μM; 16 h) induces the synthesis of HO-1 protein in a concentration-dependent fashion.[2] 8-Bromo-cGMP sodium (1-100 μM; 8 h) increases the resistance of LLC-PK1 cells to CsA toxicity in concentration-dependently.[2]
体内活性: 8-Bromo-cGMP sodium (0.3, 1, 3 nM; intrathecal administration; 10 min before the test; male ICR mice) significantly increases the tail-flick latency in Vincristine-treated mice to the level observed in vehicle-treated naive mice in dose-dependently.[3] 8-Bromo-cGMP sodium (10 mg/kg; iv; single dose) results in vasodilator responses in WT littermates and eNOS-Tg mice in C57BL/6 background (19-35 g).[4]
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 (201.8 mM)
关键字: 8 Bromo cGMP sodium | 8-Bromo-cGMP sodium | 8BromocGMP sodium
相关产品: 4-Hydroxycinnamamide | NecroX-5 | Calcicludine | Alismol | AY 77 | (R)-(+)-Bay-K-8644 | Atagabalin HCl | CRAC intermediate 1 | SKF-96365 hydrochloride | Periplocymarin
相关库: Membrane Protein-targeted Compound Library | Bioactive Compounds Library Max | Kinase Inhibitor Library | Tyrosine Kinase Inhibitor 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