Tepirindole

From WikiMD.com - Food, Medicine & Wellness Encyclopedia

A reversible inhibitor of monoamine oxidase A


Tepirindole
[[File:
Chemical structure of Tepirindole
|frameless|220px|alt=|]]
INN
Drug class
Routes of administration
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status
CAS Number 24139-02-6
PubChem 3047805
DrugBank
ChemSpider 2310100
KEGG D06078


Tepirindole is a pharmaceutical compound classified as a reversible inhibitor of monoamine oxidase A (RIMA). It is primarily used in the treatment of depression, particularly in cases where patients do not respond adequately to other antidepressant medications.

Pharmacology[edit | edit source]

Tepirindole functions by selectively inhibiting the enzyme monoamine oxidase A (MAO-A), which is responsible for the breakdown of monoamines such as serotonin, norepinephrine, and dopamine. By inhibiting this enzyme, tepirindole increases the availability of these neurotransmitters in the synaptic cleft, thereby enhancing mood and alleviating symptoms of depression.

Unlike traditional monoamine oxidase inhibitors (MAOIs), tepirindole is a reversible inhibitor, meaning it temporarily binds to the enzyme and can be displaced by high concentrations of substrate. This property reduces the risk of hypertensive crisis associated with dietary tyramine intake, a common concern with irreversible MAOIs.

Clinical Use[edit | edit source]

Tepirindole is indicated for the treatment of major depressive disorder, particularly in patients who have not responded to other treatments. Its use is less common compared to other antidepressants, and it is typically considered when other options have failed or are contraindicated.

Side Effects[edit | edit source]

Common side effects of tepirindole include nausea, dizziness, and insomnia. As with other MAOIs, there is a potential for drug interactions, and patients are advised to avoid certain medications and foods high in tyramine.

Mechanism of Action[edit | edit source]

The mechanism of action of tepirindole involves the selective and reversible inhibition of MAO-A. This enzyme is primarily responsible for the catabolism of serotonin and norepinephrine, neurotransmitters that play a crucial role in mood regulation. By inhibiting MAO-A, tepirindole increases the levels of these neurotransmitters, thereby exerting its antidepressant effects.

Chemical Properties[edit | edit source]

Tepirindole is chemically known as 5,6,7,8-tetrahydro-1,2,3,4-tetrahydroacridin-9-amine. It is a derivative of acridine, a compound known for its diverse biological activities. The chemical structure of tepirindole is characterized by a tricyclic ring system, which is common among many antidepressant agents.

Related Pages[edit | edit source]

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD