NH-3是一种具有口服活性的、可逆的甲状腺激素受体 (THR) 拮抗剂,IC50 值为 55 nM。它是选择性甲状腺素 GC-1 的衍生物,能够阻止甲状腺激素与其受体的结合,并抑制辅因子的招募。
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描述 | NH-3 is an orally active, reversible thyroid hormone receptor (THR) antagonist with an IC50 of 55 nM. It is derived from the selective thyromimetic GC-1 and inhibits the binding of thyroid hormones to their receptor as well as cofactor recruitment[1][2][3]. NH-3 serves as a click chemistry reagent, containing an Alkyne group capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. |
体内研究 | NH3 (46.2-27,700 nmol/kg/day; 7 days) modestly reduces heart rate starting at 46.2 nmol/kg/day, with the effect disappearing at doses exceeding 2920 nmol/kg/day. NH3 does not impact the cholesterol-lowering activity of T3 at a dose of 46.2 nmol/kg/day, but it inhibits tachycardia and suppresses TSH up to a dose of 924 nmol/kg/day[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.11mL 0.42mL 0.21mL |
10.56mL 2.11mL 1.06mL |
21.12mL 4.22mL 2.11mL |
CAS号 | 447415-26-1 |
分子式 | C28H27NO6 |
分子量 | 473.517 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
溶解度 |
DMSO: 105 mg/mL(221.74 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |