Temocaprilum

Temocaprilum Uses, Dosage, Side Effects, Food Interaction and all others data.

Temocaprilum is a prodrug-type angiotensin-I converting enzyme (ACE) inhibitor not approved for use in the United States, but is approved in Japan and South Korea. Temocaprilum can also be used in hemodialysis patients without risk of serious accumulation.

Temocaprilum is a prodrug of its active metabolite (and diacid form) temocaprilat which contains a thiazepine ring. Temocaprilumat has slightly higher potency than enalaprilat in ACE inhibition isolated from rabbit lung. ACE inhibitors exert their hemodynamic effect mainly by inhibiting the renin-angiotensin system. They also modulate sympathetic nervous system activity and increase prostaglandin synthesis. They cause mainly vasodilation and mild natriuresis without affecting heart rate and contractility.). When compared with other Angiotensin-converting Enzyme Inhibitors, temocapril's advantages include a rapid onset of action and what research suggests is tighter vascular ACE binding than enalaprilat.

Table Of contents

• Temocaprilum
• Uses
• Dosage
• Side Effect
• Precautions
• Interactions
• Uses during Pregnancy
• Uses during Breastfeeding
• Accute Overdose
• Food Interaction
• Half Life
• Volume of Distribution
• Clearance
• Interaction With other Medicine
• Contradiction
• Storage

Trade Name	Temocaprilum
Generic	Temocapril
Temocapril Other Names	Temocapril, Temocaprilum
Type
Formula	C23H28N2O5S2
Weight	Average: 476.609 Monoisotopic: 476.143963396
Protein binding	99.5%, including those with renal impairment.
Groups	Experimental, Investigational
Therapeutic Class
Manufacturer
Available Country
Last Updated:	September 19, 2023 at 7:00 am

Uses

Temocaprilum is an ACE inhibitor primarily indicated in the treatment of hypertension and congestive heart failure, diabetic nephropathy, and improvement of prognosis for coronary artery diseases (including acute myocardial infarction).

Toxicity

In rats, whether or male or female, the LD50 values of temocapril were higher than 5000 mg/kg.

Elimination Route

Temocaprilum is rapidly absorbed in the gastrointestinal tract and converted into the diacid (active) metabolite, which inhibits ACE in plasma.

Half Life

13.1 hours in patients with normal liver function.

Clearance

19.4% urinary recovery.

Elimination Route

Temocaprilum is eliminated primarily through the liver and kidneys.

Innovators Monograph

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