用户名: 密   码:
注册 | 忘记密码?
药品详细

Practolol(心得宁)

化学结构式图
中文名
心得宁
英文名
Practolol
分子式
C14H22N2O3
化学名
N-(4-{2-hydroxy-3-[(propan-2-yl)amino]propoxy}phenyl)acetamide
分子量
Average: 266.3361
Monoisotopic: 266.16304258
CAS号
6673-35-4
ATC分类
C07A 未知
药物类型
small molecule
阶段
approved
商品名
同义名
基本介绍

A beta-adrenergic antagonist that has been used in the emergency treatment of cardiac arrhythmias. [PubChem]

生产厂家
    封装厂家
    参考
    Synthesis Reference Not Available
    General Reference Not Available
    剂型
    规格
    化合物类型
    Type small molecule
    Classes Not Available
    Substructures Not Available
    适应症
    药理
    Indication Used in the emergency treatment of cardiac arrhythmias.
    Pharmacodynamics Practolol is a beta-adrenergic receptor antagonist that has been used in the emergency treatment of cardiac arrhythmias. Beta blockers inhibit normal epinephrine-mediated sympathetic actions, but have minimal effect on resting subjects. That is, they reduce the effect of excitement/physical exertion on heart rate and force of contraction and dilation of blood vessels.
    Mechanism of action Like other beta-adrenergic antagonists, practolol competes with adrenergic neurotransmitters such as catecholamines for binding at sympathetic receptor sites. Like propranolol and timolol, practolol binds at beta(1)-adrenergic receptors in the heart and vascular smooth muscle, inhibiting the effects of the catecholamines epinephrine and norepinephrine and decreasing heart rate, cardiac output, and systolic and diastolic blood pressure.
    Absorption Not Available
    Volume of distribution Not Available
    Protein binding Not Available
    Metabolism
    Not Available
    Route of elimination Not Available
    Half life Not Available
    Clearance Not Available
    Toxicity Symptoms of overdose include abdominal irritation, central nervous system depression, coma, extremely slow heartbeat, heart failure, lethargy, low blood pressure, and wheezing.
    Affected organisms Not Available
    Pathways Not Available
    理化性质
    Properties
    State solid
    Experimental Properties
    Property Value Source
    melting point 134-136 °C PhysProp
    logP 0.79 HANSCH,C ET AL. (1995)
    Caco2 permeability -6.05 ADME Research, USCD
    Predicted Properties
    Property Value Source
    water solubility 4.90e-01 g/l ALOGPS
    logP 0.53 ALOGPS
    logP 0.83 ChemAxon
    logS -2.7 ALOGPS
    pKa (strongest acidic) 14.03 ChemAxon
    pKa (strongest basic) 9.67 ChemAxon
    physiological charge 1 ChemAxon
    hydrogen acceptor count 4 ChemAxon
    hydrogen donor count 3 ChemAxon
    polar surface area 70.59 ChemAxon
    rotatable bond count 7 ChemAxon
    refractivity 75.24 ChemAxon
    polarizability 30.39 ChemAxon
    药物相互作用
    Drug Interaction
    Acetohexamide The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Chlorpropamide The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Clonidine Increased hypertension when clonidine stopped
    Dihydroergotamine Ischemia with risk of gangrene
    Disopyramide The beta-blocker, practolol, may increase the toxicity of disopyramide.
    Epinephrine Hypertension, then bradycardia
    Ergotamine Ischemia with risk of gangrene
    Fenoterol Antagonism
    Formoterol Antagonism
    Gliclazide The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Glyburide The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Ibuprofen Risk of inhibition of renal prostaglandins
    Indomethacin Risk of inhibition of renal prostaglandins
    Insulin Glargine The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Methysergide Ischemia with risk of gangrene
    Orciprenaline Antagonism
    Oxprenolol Antagonism
    Pipobroman Antagonism
    Piroxicam Risk of inhibition of renal prostaglandins
    Prazosin Risk of hypotension at the beginning of therapy
    Repaglinide The beta-blocker, practolol, may decrease symptoms of hypoglycemia.
    Terbutaline Antagonism
    食物相互作用
    • Avoid alcohol.
    • Avoid natural licorice.

    返回 | 收藏