2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine
非肽类血管紧张素II受体拮抗剂
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 100mg | 请咨询 | 现货 | |
| 250mg | 请咨询 | 现货 | |
| 500mg | 请咨询 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine is a nonpeptidic angiotensin II receptor antagonist.
Angiotensin II is the critical pressor substance of the renin-angiotensin system (RAS). The angiotensin II system, a proteolytic cascade regulating hemodynamics and water and electrolyte balance, is able to contribute to hypertensive states in human. The effects of the octapeptide angiotensin I1 includs cardiac stimulation, vasoconstriction, stimulation of aldosterone synthesis and release, as well as renal reabsorption of sodium.
In vitro: In a previous study, 2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine was synthezed by reduction of 2-amino-3-nitropyridine derivatives to the corresponding diaminopyridine which was then condensed with an appropriate carboxylic acid in polyphosphoric acid. In vitro activity study showed that 2-Ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine was a nonpeptidic angiotensin II receptor antagonist whose imidazo[4,5-b]pyridine scaffold had been used to examine plenty of positional substitutions in the development of orally active, long duration antihypertensive agents [1].
In vivo: Up to now, there is no animal in vivo data reported.
Clinical trial: So far, no clinical study has been conducted.
Reference:
[1] Mantlo, N. B.,Chakravarty, P.K.,Ondeyka, D.L., et al. Potent, orally active Imadazo[4,5-b]pyridine-based angiotensin II receptor antagonists. Journal of Medicinal Chemistry 34(9), 2919-2922 (1991).
产品性质
| CAS号 | 133240-06-9 |
| 分子式 | C10H13N3 |
| 分子量 | 175.2 |
| 化学名称 | 2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine |
| 溶解度 | insoluble in H2O; ≥45.7 mg/mL in EtOH; ≥5.3 mg/mL in DMSO |
| SMILES | CCC1=NC2=C(C)C=C(C)NC2=N1 |
| 存储条件 | -20°C |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 腺苷受体拮抗剂 4(化合物 2)是一种腺苷 A1 受体拮抗剂;对人类 A1 受体的 Ki 值为 101 nM。 |
| 靶点 | Angiotensin Receptor |



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