Cloperastine hydrochloride
CAS No. 14984-68-0
Cloperastine hydrochloride ( —— )
产品货号. M12081 CAS No. 14984-68-0
盐酸氯哌斯汀是一种黄酮,黄酮类化合物的一种。与所有类黄酮一样,它具有黄色结晶外观。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 500MG | ¥133 | 有现货 |
|
| 1G | ¥188 | 有现货 |
|
| 1 mL x 10 mM in DMSO | ¥147 | 有现货 |
|
生物学信息
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产品名称Cloperastine hydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述盐酸氯哌斯汀是一种黄酮,黄酮类化合物的一种。与所有类黄酮一样,它具有黄色结晶外观。
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产品描述Cloperastine hydrochloride is a flavone, a type of flavonoid. Like all flavonoids, it has a yellow crystalline appearance.(In Vitro):Cloperastine inhibits the hERG K+ currents in a concentrationdependent manner with an IC50 value of 27 nM.Among the antitussive agents, Cloperastine, which possesses antitussive and antiedemic activity, also relaxes the bronchial musculature. Cloperastine is a drug with a central antitussive effect, and is also endowed with an antihistaminic and papaverine-like activity similar to codeine but without its narcotic effects.(In Vivo):In the anesthetized guinea pigs, Cloperastine at a therapeutic dose of 1 mg/kg prolonged the QT interval and monophasic action potential (MAP) duration without affecting PR interval or QRS width.Cloperastine hydrochloride shows relatively low acute toxicity when administered by the intraperitoneal route in rats and mice, and shows minor toxicity by the oral route when administered as Cloperastine fendizoate, the LD50 in rats and mice for the two administration routes exceeds 1000 and 2000 mg/kg, respectively.
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体外实验——
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体内实验——
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同义词——
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通路Endocrinology/Hormones
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靶点5-HT Receptor
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受体HT
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研究领域——
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适应症——
化学信息
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CAS Number14984-68-0
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分子量366.33
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分子式C20H25Cl2NO
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纯度>98% (HPLC)
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溶解度Soluble in DMSO
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SMILESCl.ClC1=CC=C(C=C1)C(OCCN1CCCCC1)C1=CC=CC=C1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Yu MC, et al. Eur J Pharmacol, 2010, 627(1-3), 269-275.
产品手册
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