Nepicastat: Difference between revisions
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{{Short description|An article about the drug Nepicastat}} | |||
{{Drugbox | |||
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| verifiedrevid = 477002123 | |||
| IUPAC_name = 2-[(2S)-2-hydroxy-2-phenylethyl]hydrazinecarboximidamide | |||
| image = Nepicastat_Structure.svg | |||
| image_size = 200px | |||
}} | |||
'''Nepicastat''' is a [[pharmacological]] agent that acts as a selective inhibitor of the enzyme [[dopamine beta-hydroxylase]] (DBH). This enzyme is responsible for the conversion of [[dopamine]] to [[norepinephrine]], a key neurotransmitter in the [[sympathetic nervous system]]. | |||
Nepicastat | |||
== | ==Mechanism of Action== | ||
Nepicastat | Nepicastat inhibits the activity of dopamine beta-hydroxylase, thereby reducing the synthesis of norepinephrine. This reduction in norepinephrine levels can lead to decreased [[sympathetic nervous system]] activity, which may be beneficial in conditions characterized by excessive sympathetic activity. | ||
==Therapeutic Uses== | |||
Nepicastat has been investigated for its potential use in the treatment of various conditions, including: | |||
* [[Congestive heart failure]] | |||
* [[Post-traumatic stress disorder]] (PTSD) | |||
* [[Hypertension]] | |||
== | By modulating norepinephrine levels, Nepicastat may help alleviate symptoms associated with these conditions. | ||
==Pharmacokinetics== | |||
Nepicastat is administered orally and undergoes hepatic metabolism. The pharmacokinetic profile of Nepicastat includes its absorption, distribution, metabolism, and excretion, which are important for determining the appropriate dosing regimen. | |||
==Side Effects== | |||
Common side effects of Nepicastat may include: | |||
* [[Dizziness]] | |||
* [[Fatigue]] | |||
* [[Nausea]] | |||
These side effects are generally mild and may diminish with continued use. | |||
==Research and Development== | |||
Research into Nepicastat is ongoing, with studies focusing on its efficacy and safety in various clinical settings. The drug's ability to modulate norepinephrine levels makes it a promising candidate for further investigation. | |||
==Related pages== | |||
* [[Dopamine beta-hydroxylase]] | * [[Dopamine beta-hydroxylase]] | ||
* [[ | * [[Norepinephrine]] | ||
* [[ | * [[Sympathetic nervous system]] | ||
[[Category:Drugs]] | [[Category:Drugs]] | ||
[[Category: | [[Category:Enzyme inhibitors]] | ||
[[Category: | [[Category:Sympatholytics]] | ||
Latest revision as of 11:36, 15 February 2025
An article about the drug Nepicastat
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Nepicastat is a pharmacological agent that acts as a selective inhibitor of the enzyme dopamine beta-hydroxylase (DBH). This enzyme is responsible for the conversion of dopamine to norepinephrine, a key neurotransmitter in the sympathetic nervous system.
Mechanism of Action[edit]
Nepicastat inhibits the activity of dopamine beta-hydroxylase, thereby reducing the synthesis of norepinephrine. This reduction in norepinephrine levels can lead to decreased sympathetic nervous system activity, which may be beneficial in conditions characterized by excessive sympathetic activity.
Therapeutic Uses[edit]
Nepicastat has been investigated for its potential use in the treatment of various conditions, including:
By modulating norepinephrine levels, Nepicastat may help alleviate symptoms associated with these conditions.
Pharmacokinetics[edit]
Nepicastat is administered orally and undergoes hepatic metabolism. The pharmacokinetic profile of Nepicastat includes its absorption, distribution, metabolism, and excretion, which are important for determining the appropriate dosing regimen.
Side Effects[edit]
Common side effects of Nepicastat may include:
These side effects are generally mild and may diminish with continued use.
Research and Development[edit]
Research into Nepicastat is ongoing, with studies focusing on its efficacy and safety in various clinical settings. The drug's ability to modulate norepinephrine levels makes it a promising candidate for further investigation.