Minaprine: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 1: Line 1:
'''Minaprine''' is a [[reversible inhibitor of monoamine oxidase A]] (RIMA), a type of [[antidepressant]], that was introduced in [[France]] in the 1970s for the treatment of [[depression]].
== Minaprine ==


==Pharmacology==
[[File:Minaprine.svg|thumb|right|Chemical structure of Minaprine]]
Minaprine acts as a [[reversible inhibitor]] of [[monoamine oxidase A]] (MAO-A), an enzyme that breaks down [[monoamines]] in the body. By inhibiting MAO-A, minaprine increases the levels of these monoamines, which include [[serotonin]], [[norepinephrine]], and [[dopamine]]. This increase in monoamines is thought to be responsible for the antidepressant effects of minaprine.


==Clinical use==
'''Minaprine''' is a psychotropic drug that was primarily used as an [[antidepressant]] in the treatment of [[major depressive disorder]]. It was developed in the 1980s and marketed in several countries, although it is not widely used today. Minaprine is known for its unique pharmacological profile, which includes both [[monoamine oxidase inhibition]] and [[serotonin receptor]] modulation.
Minaprine was introduced in France in the 1970s for the treatment of depression. It has also been used to treat [[anxiety disorders]], [[cognitive impairment]], and [[fatigue]]. However, its use has declined in recent years due to the development of newer antidepressants with fewer side effects.


==Side effects==
== Pharmacology ==
The most common side effects of minaprine include [[nausea]], [[dizziness]], and [[insomnia]]. In rare cases, it can cause [[hypertensive crisis]], a serious condition characterized by extremely high blood pressure.


==See also==
Minaprine acts as a reversible inhibitor of [[monoamine oxidase A]] (RIMA), which is an enzyme responsible for the breakdown of [[monoamines]] such as [[serotonin]], [[norepinephrine]], and [[dopamine]]. By inhibiting this enzyme, Minaprine increases the levels of these neurotransmitters in the brain, which can help alleviate symptoms of depression.
 
In addition to its action on monoamine oxidase, Minaprine also interacts with various [[serotonin receptors]], particularly the [[5-HT2]] receptor. This interaction is thought to contribute to its antidepressant effects and may also influence its side effect profile.
 
== Clinical Use ==
 
Minaprine was used in the treatment of major depressive disorder, particularly in cases where patients did not respond to other antidepressants. It was considered to have a relatively favorable side effect profile compared to some other antidepressants available at the time.
 
== Side Effects ==
 
Common side effects of Minaprine included [[nausea]], [[headache]], and [[insomnia]]. Some patients also reported [[dizziness]] and [[dry mouth]]. As with other antidepressants, there was a risk of [[serotonin syndrome]] if Minaprine was taken in combination with other serotonergic drugs.
 
== Synthesis ==
 
[[File:Minaprine_synthesis_1989.svg|thumb|left|Synthesis of Minaprine]]
 
The synthesis of Minaprine involves several chemical reactions starting from basic organic compounds. The process typically includes the formation of the core structure followed by the addition of various functional groups to achieve the final active compound. The detailed synthesis pathway is illustrated in the accompanying diagram.
 
== Discontinuation ==
 
Minaprine was eventually withdrawn from the market in several countries due to concerns about its safety and the availability of newer antidepressants with improved efficacy and safety profiles. However, it remains a compound of interest in pharmacological research due to its unique mechanism of action.
 
== Related Pages ==
 
* [[Antidepressant]]
* [[Monoamine oxidase inhibitor]]
* [[Monoamine oxidase inhibitor]]
* [[Antidepressant]]
* [[Serotonin]]
* [[Depression (mood)]]
* [[Major depressive disorder]]


[[Category:Antidepressants]]
[[Category:Antidepressants]]
[[Category:Monoamine oxidase inhibitors]]
[[Category:Monoamine oxidase inhibitors]]
{{pharma-stub}}
<gallery>
File:Minaprine.svg|Minaprine
File:Minaprine synthesis 1989.svg|Minaprine synthesis 1989
</gallery>
<gallery>
File:Minaprine synthesis 1989.svg|Minaprine synthesis 1989
</gallery>

Latest revision as of 10:53, 23 March 2025

Minaprine[edit]

Chemical structure of Minaprine

Minaprine is a psychotropic drug that was primarily used as an antidepressant in the treatment of major depressive disorder. It was developed in the 1980s and marketed in several countries, although it is not widely used today. Minaprine is known for its unique pharmacological profile, which includes both monoamine oxidase inhibition and serotonin receptor modulation.

Pharmacology[edit]

Minaprine acts as a reversible inhibitor of monoamine oxidase A (RIMA), which is an enzyme responsible for the breakdown of monoamines such as serotonin, norepinephrine, and dopamine. By inhibiting this enzyme, Minaprine increases the levels of these neurotransmitters in the brain, which can help alleviate symptoms of depression.

In addition to its action on monoamine oxidase, Minaprine also interacts with various serotonin receptors, particularly the 5-HT2 receptor. This interaction is thought to contribute to its antidepressant effects and may also influence its side effect profile.

Clinical Use[edit]

Minaprine was used in the treatment of major depressive disorder, particularly in cases where patients did not respond to other antidepressants. It was considered to have a relatively favorable side effect profile compared to some other antidepressants available at the time.

Side Effects[edit]

Common side effects of Minaprine included nausea, headache, and insomnia. Some patients also reported dizziness and dry mouth. As with other antidepressants, there was a risk of serotonin syndrome if Minaprine was taken in combination with other serotonergic drugs.

Synthesis[edit]

Synthesis of Minaprine

The synthesis of Minaprine involves several chemical reactions starting from basic organic compounds. The process typically includes the formation of the core structure followed by the addition of various functional groups to achieve the final active compound. The detailed synthesis pathway is illustrated in the accompanying diagram.

Discontinuation[edit]

Minaprine was eventually withdrawn from the market in several countries due to concerns about its safety and the availability of newer antidepressants with improved efficacy and safety profiles. However, it remains a compound of interest in pharmacological research due to its unique mechanism of action.

Related Pages[edit]