Alprenolol
CAS No. 13655-52-2
Alprenolol ( (RS)-Alprenolol | dl-Alprenolol )
产品货号. M17974 CAS No. 13655-52-2
Alprenolol 是一种非选择性 β-肾上腺素能受体 (β-AR) 拮抗剂,也是血清素 (5-HT) 受体亚型 5-HT1A 和 5-HT1B 的拮抗剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥564 | 有现货 |
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| 100MG | 获取报价 | 有现货 |
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| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Alprenolol
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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Alprenolol 是一种非选择性 β-肾上腺素能受体 (β-AR) 拮抗剂,也是血清素 (5-HT) 受体亚型 5-HT1A 和 5-HT1B 的拮抗剂。
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产品描述Alprenolol is a non-selective β-adrenergic receptor (β-AR) antagonist that is also an antagonist of the serotonin (5-HT) receptor subtypes 5-HT1A and 5-HT1B.(In Vivo):heart rate by 39 beats/min (at 3-hr) in conscious renal hypertensive dogs.Alprenolol (i.p., 5 mg/kg) effectively blockes the anxiolytic effects of indorenate and ipsapirone but do not reduce the motor activity in adult male Swiss Webster mice.Alprenolol (intravenous injection, 0.5 or 1.0 mg/kg) can decrease systolic pressure by a mean of 10 mm Hg, diastolic pressure by a mean of 10 mm Hg) and heart rate by 23 beats/min, as well as slightly reduce both myocardial and liver blood flows by mean of 17% and 15% respectively at a dose of 1.0 mg/kg in cats.
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体外实验——
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体内实验Alprenolol (p.o., 50 mg/kg) causes a significant drop in blood pressure which averages 20 mm Hg (at 3-hr) and an increase in heart rate by 39 beats/min (at 3-hr) in conscious renal hypertensive dogs.Alprenolol (i.p., 5 mg/kg) effectively blockes the anxiolytic effects of indorenate and ipsapirone but do not reduce the motor activity in adult male Swiss Webster mice.Alprenolol (intravenous injection, 0.5 or 1.0 mg/kg) can decrease systolic pressure by a mean of 10 mm Hg, diastolic pressure by a mean of 10 mm Hg) and heart rate by 23 beats/min, as well as slightly reduce both myocardial and liver blood flows by mean of 17% and 15% respectively at a dose of 1.0 mg/kg in cats.
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同义词(RS)-Alprenolol | dl-Alprenolol
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通路Chromatin/Epigenetic
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靶点Epigenetic Reader Domain
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受体β-adrenergic receptor| 5-HT
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研究领域Cancer
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适应症——
化学信息
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CAS Number13655-52-2
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分子量249.35
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分子式C15H23NO2
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 100 mg/mL 401.04 mM; H2O : < 0.1 mg/mL
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SMILESCC(C)NCC(O)COc1ccccc1CC=C
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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. Baker, J.G. The selectivity of β-adrenoceptor antagonists at the human β1, β2 and β3 adrenoceptors. Br. J. Pharmacol. 144(3), 317-322 (2005).
产品手册
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