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NH-3是一种高效的口服活性甲状腺激素受体(THR)拮抗剂,具有可逆行为,其IC 50为55 nM。NH-3源自选择性甲状腺激素模拟物GC-1,有效地抑制甲状腺激素与相应受体的结合,从而阻碍辅因子的招募。
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NH-3是一种高效的口服活性甲状腺激素受体(THR)拮抗剂,具有可逆行为,其IC 50为55 nM。NH-3源自选择性甲状腺激素模拟物GC-1,有效地抑制甲状腺激素与相应受体的结合,从而阻碍辅因子的招募。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 2,290 | 现货 | |
5 mg | ¥ 4,630 | 现货 | |
10 mg | ¥ 6,490 | 现货 | |
25 mg | ¥ 9,630 | 现货 | |
50 mg | ¥ 12,900 | 现货 | |
100 mg | ¥ 17,500 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 4,830 | 现货 |
产品描述 | NH-3 is a potent orally active thyroid hormone receptor (THR) antagonist which exhibits reversible behavior, demonstrated by an IC 50 of 55 nM. Derived from the selective thyromi-metic GC-1, NH-3 effectively inhibits the binding of thyroid hormones to their respective receptors, resulting in hindered cofactor recruitment. |
靶点活性 | THR:55 nM (IC50) |
体内活性 | NH3(46.2-27,700 nmol/kg/day;7天)从46.2 nmol/kg/day开始使心率适度降低,但在>2920 nmol/kg/day时效果消失。NH3对46.2 nmol/kg/day T3的降胆固醇作用无影响,但它抑制了心动过速和TSH抑制效果,直至924 nmol/kg/day剂量[2]。 |
分子量 | 473.52 |
分子式 | C28H27NO6 |
CAS No. | 447415-26-1 |
Smiles | CC(C)c1cc(Cc2c(C)cc(OCC(O)=O)cc2C)cc(C#Cc2ccc(cc2)[N+]([O-])=O)c1O |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 95 mg/mL (200.63 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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