CAS NO: | 107220-28-0 |
生物活性 | Cevimeline hydrochloride (AF102B hydrochloride) is a quinuclidine derivative of acetylcholine and a selective and orally activemuscarinic M1 and M3 receptoragonist. Cevimeline hydrochloride stimulates secretion by the salivary glands and can be used as a sialogogue for xerostomia[1][2][3][4]. Cevimeline hydrochloride can cross the blood-brain barrier (BBB)[5]. | ||||||||||||||||
IC50& Target | Muscarinic M1 and M3 receptor[1] | ||||||||||||||||
体外研究 (In Vitro) | In digested parotid cells, Cevimeline (0.1-100 μM) increases the intracellular Ca2+concentration[1]. | ||||||||||||||||
体内研究 (In Vivo) | Cevimeline (0.008-0.016 mg/kg; intraperitoneal injection; male Wistar rats) treatment shows slowly increasing and lasting salivation, and increased blood flow increment in the parotid gland and pressor response. Cevimeline inhibits angiotensin II-induced water intake and neuronal activity in the subfornical organ at 0.016 mg/kg[1].
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Clinical Trial | |||||||||||||||||
分子量 | 235.77 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C10H18ClNOS | ||||||||||||||||
CAS 号 | 107220-28-0 | ||||||||||||||||
中文名称 | 盐酸西维美林 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: H2O : ≥ 50 mg/mL(212.07 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 |
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