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分子式 C13H19N5 · H2O 分子量263.34 Beilstein号 EC号 262-294-9 MDL号 MFCD00242745 PubChem编号 24277866 属性 溶解性 Soluble in 100% ethano
| 货号 | CAS号 | 操作 |
|---|---|---|
| P130092-500mg | 85371-64-8 | 询底价 |
| P130092-100mg | 85371-64-8 | 询底价 |
耗材描述
- 分子式 C13H19N5 · H2O
- 分子量263.34
- Beilstein号
- EC号 262-294-9
- MDL号 MFCD00242745
- PubChem编号 24277866
属性
| 溶解性 | Soluble in 100% ethanol (14 mg/ml), DMSO (15 mg/ml), dilute aqueous acid, and 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin (40 mg/ml). Insoluble in water |
描述
| 应用 | A K+ channel activator; antihypertensive |
| 产品介绍 | Pinacidil is a K+ channel opener. Pinacidil is demonstrated to induce relaxation of serotonin-produced contractions in porcine and human arterial rings. This action is suppressed by the ATP-dependent K+ (KATP) channel blockers Glibenclamide and Tetrapentylammonium salts, suggesting that relaxations induced by Pinacidil are mediated by opening of KATP channels. |
| 别名 | (±)-N-氰基-N'-4-吡啶基-N''-(1,2,2-三甲基丙基)胍;(±)-N-Cyano-N′-4-pyridinyl-N″-(1,2,2-trimethylpropyl)guanidine monohydrate |
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