プロカインアミド

プロカインアミド 化学構造式
51-06-9
CAS番号.
51-06-9
化学名:
プロカインアミド
别名:
4-アミノ-N-[2-(ジエチルアミノ)エチル]ベンズアミド;プロカミド;p-アミノ-N-(2-ジエチルアミノエチル)ベンズアミド;プロカインアミド;p-アミノ-N-[2-(ジエチルアミノ)エチル]ベンズアミド;ノボカインアミド;プロカイナミド;N-[2-(ジエチルアミノ)エチル]-4-アミノベンズアミド;ノボカミド
英語名:
procainamide
英語别名:
C07401;Procamide;Novocamid;Procainamide;Novocainamide;PROCAINEAMIDE;Novocaine amide;procainamide USP/EP/BP;procainamide Solution, 100ppm;4-Amino-N-(2-diethylaminoethyl)
CBNumber:
CB5932746
化学式:
C13H21N3O
分子量:
235.33
MOL File:
51-06-9.mol

プロカインアミド 物理性質

融点 :
47°C
沸点 :
377.72°C (rough estimate)
比重(密度) :
1.060
屈折率 :
1.5700 (estimate)
貯蔵温度 :
Keep in dark place,Inert atmosphere,Room temperature
溶解性:
クロロホルム(微量)、酢酸エチル(微量)
外見 :
個体
酸解離定数(Pka):
pKa 9.24±0.10 (Uncertain)
色:
オフホワイトからライトブラウン

安全性情報

RIDADR  2811
国連危険物分類  6.1
容器等級 
有毒物質データの 51-06-9(Hazardous Substances Data)

プロカインアミド 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

プロカインアミド 化学特性,用途語,生産方法

効能

抗不整脈薬, ナトリウムチャネル遮断薬

説明

Procainamide and its analogs were employed by Dr Claude Beck in a series of cardiac surgeries during the early 1930s. The compound was used to alleviate arrhythmias that present during the procedures, and was selected for its favorable tissue absorption properties. Procainamide’s central amide provides it protection from inactivating esterase action and allows oral administration of the compound. Procainamide was approved for use in the United States in 1950.

使用

Procainamide is intended for treating paroxysmal atrial tachycardia, atrial fibrillation, premature ventricular contraction, and ventricular tachycardia. For quickly reaching therapeutic concentrations, parenternal introduction of procainamide is preferred over cynidine.

定義

ChEBI: 4-Aminobenzamide substituted on the amide N by a 2-(diethylamino)ethyl group. It is a pharmaceutical antiarrhythmic agent used for the medical treatment of cardiac arrhythmias.

生物学の機能

Procainamide (Pronestyl, Procan SR) is a derivative of the local anesthetic agent procaine. Procainamide has a longer half-life, does not cause CNS toxicity at therapeutic plasma concentrations, and is effective orally. Procainamide is a particularly useful antiarrhythmic drug, effective in the treatment of supraventricular, ventricular, and digitalis-induced arrhythmias.

作用機序

The chemical difference between procainamide and procaine lies in the replacement of the ester group with an amide group. The action of procainamide is qualitatively similar to the action of procaine. Its effect on the heart is identical to that of quinidine. As an antiarrhythmic, procainamide is preferred over procaine because unlike procaine, it is better absorbed when taken orally and it is more difficult for the esterases of the plasma to hydrolyze it, which results in long-lasting action.

臨床応用

Procainamide is an effective antiarrhythmic agent when given in sufficient doses at relatively short (3–4 hours) dosage intervals. Procainamide is useful in the treatment of premature atrial contractions, paroxysmal atrial tachycardia, and atrial fibrillation of recent onset. Procainamide is only moderately effective in converting atrial flutter or chronic atrial fibrillation to sinus rhythm, although it has value in preventing recurrences of these arrhythmias once they have been terminated by direct current (DC) cardioversion.
Procainamide can decrease the occurrence of all types of active ventricular dysrhythmias in patients with acute myocardial infarction who are free from A-V dissociation, serious ventricular failure, and cardiogenic shock. About 90% of patients with ventricular premature contractions and 80% of patients with ventricular tachycardia respond to procainamide administration. Although the spectrum of action and electrophysiological effects of quinidine and procainamide are similar, the relatively short duration of action of procainamide has tended to restrict its use to patients who are intolerant of or unresponsive to quinidine.

副作用

Acute cardiovascular reactions to procainamide administration include hypotension, A-V block, intraventricular block, ventricular tachyarrhythmias, and complete heart block. The drug dosage must be reduced or even stopped if severe depression of conduction (severe prolongation of the QRS interval) or repolarization (severe prolongation of the QT interval) occurs.
Long-term drug use leads to increased antinuclear antibody titers in more than 80% of patients; more than 30% of patients receiving long-term procainamide therapy develop a clinical lupus erythematosus–like syndrome. The symptoms may disappear within a few days of cessation of procainamide therapy, although the tests for antinuclear factor and lupus erythematosus cells may remain positive for several months.
Procainamide, unlike procaine, has little potential to produce CNS toxicity. Rarely, patients may be confused or have hallucinations.

薬物相互作用

The inherent anticholinergic properties of procainamide may interfere with the therapeutic effect of cholinergic agents. Patients receiving cimetidine and procainamide may exhibit signs of procainamide toxicity, as cimetidine inhibits the metabolism of procainamide. Simultaneous use of alcohol will increase the hepatic clearance of procainamide. Procainamide may enhance or prolong the neuromuscular blocking activity of the aminoglycosides with the potential of producing respiratory depression. The simultaneous administration of quinidine or amiodarone may increase the plasma concentration of procainamide.

代謝

Metabolites of procainamide include p-aminobenzoic acid and N-acetylprocainamide. Interestingly, the acetylated metabolite is also active as an antiarrhythmic. Its formation accounts for up to one-third of the administered dose and is catalyzed by the liver enzyme N-acetyl transferase. Because acetylation is strongly influenced by an individual's genetic background, marked variability in the amounts of this active metabolite may be observed from patient to patient. Renal excretion dominates, with approximately 90% of a dose excreted as unchanged drug and metabolites. The elimination half-life is approximately 3.5 hours. A substantial percentage (60–70%) of patients on procainamide show elevated levels of antinuclear antibodies after a few months. Of these patients, between 20 and 30% develop a drug-induced lupus syndrome if therapy is continued. These adverse effects, which are attributed to the aromatic amino group, are observed more frequently and more rapidly in “slow acetylators.” Usually, the symptoms associated with procainamide-induced lupus syndrome subside fairly rapidly after the drug is discontinued. These problems, however, have discouraged long-term procainamide therapy.

予防処置

Contraindications to procainamide are similar to those for quinidine. Because of its effects on A-V nodal and His-Purkinje conduction, procainamide should be administered with caution to patients with second-degree A-V block and bundle branch block. Procainamide should not be administered to patients who have shown procaine or procainamide hypersensitivity and should be used with caution in patients with bronchial asthma. Prolonged administration should be accompanied by hematological studies, since agranulocytosis may occur.

プロカインアミド 上流と下流の製品情報

原材料

準備製品


プロカインアミド 生産企業

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51-06-9(プロカインアミド)キーワード:


  • 51-06-9
  • PROCAINEAMIDE
  • Novocainamide
  • Novocaine amide
  • Novocamid
  • Procamide
  • Procainamide
  • 4-Amino-N-[2-(diethylamino)ethyl]benzamide
  • C07401
  • 4-Amino-N-(2-diethylaminoethyl)
  • procainamide USP/EP/BP
  • Benzamide, 4-amino-N-[2-(diethylamino)ethyl]-
  • procainamide Solution, 100ppm
  • 4-アミノ-N-[2-(ジエチルアミノ)エチル]ベンズアミド
  • プロカミド
  • p-アミノ-N-(2-ジエチルアミノエチル)ベンズアミド
  • プロカインアミド
  • p-アミノ-N-[2-(ジエチルアミノ)エチル]ベンズアミド
  • ノボカインアミド
  • プロカイナミド
  • N-[2-(ジエチルアミノ)エチル]-4-アミノベンズアミド
  • ノボカミド
  • 抗不整脈薬
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