Velneperit: Difference between revisions
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'''Velneperit''' is a | {{Short description|A chemical compound used in medicine}} | ||
{{Use dmy dates|date=October 2023}} | |||
[[File:Velneperit.svg|thumb|Chemical structure of Velneperit]] | |||
'''Velneperit''' is a chemical compound that has been studied for its potential use in treating various medical conditions. It is known for its role as an inhibitor of the enzyme [[neutral endopeptidase]] (NEP), which is involved in the breakdown of certain peptides in the body. | |||
== | ==Chemical Properties== | ||
Velneperit is classified as a small molecule inhibitor. Its chemical structure allows it to bind to the active site of NEP, thereby preventing the enzyme from interacting with its natural substrates. This inhibition can lead to increased levels of peptides such as [[enkephalins]], which are involved in modulating pain and other physiological processes. | |||
Velneperit | ==Mechanism of Action== | ||
The primary mechanism of action of Velneperit involves the inhibition of neutral endopeptidase. By blocking NEP, Velneperit increases the concentration of peptides that are normally degraded by this enzyme. This can enhance the activity of these peptides, potentially leading to therapeutic effects in conditions where peptide regulation is disrupted. | |||
== | ==Potential Therapeutic Uses== | ||
Velneperit has been investigated for its potential use in treating conditions such as [[chronic pain]], [[hypertension]], and [[heart failure]]. The ability of Velneperit to modulate peptide levels makes it a candidate for these applications, although clinical trials are necessary to fully understand its efficacy and safety. | |||
Velneperit | ==Research and Development== | ||
Research on Velneperit has included preclinical studies and early-phase clinical trials. These studies aim to evaluate the pharmacokinetics, pharmacodynamics, and therapeutic potential of the compound. Results from these studies will determine the future development of Velneperit as a therapeutic agent. | |||
== | ==Related Pages== | ||
* [[Neutral endopeptidase]] | |||
* [[Enkephalin]] | |||
* [[Pain management]] | |||
==References== | |||
{{Reflist}} | |||
[[Category:Chemical compounds]] | |||
[[Category:Pharmacology]] | |||
[[Category:Experimental drugs]] | |||
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Revision as of 11:58, 9 February 2025
A chemical compound used in medicine

Velneperit is a chemical compound that has been studied for its potential use in treating various medical conditions. It is known for its role as an inhibitor of the enzyme neutral endopeptidase (NEP), which is involved in the breakdown of certain peptides in the body.
Chemical Properties
Velneperit is classified as a small molecule inhibitor. Its chemical structure allows it to bind to the active site of NEP, thereby preventing the enzyme from interacting with its natural substrates. This inhibition can lead to increased levels of peptides such as enkephalins, which are involved in modulating pain and other physiological processes.
Mechanism of Action
The primary mechanism of action of Velneperit involves the inhibition of neutral endopeptidase. By blocking NEP, Velneperit increases the concentration of peptides that are normally degraded by this enzyme. This can enhance the activity of these peptides, potentially leading to therapeutic effects in conditions where peptide regulation is disrupted.
Potential Therapeutic Uses
Velneperit has been investigated for its potential use in treating conditions such as chronic pain, hypertension, and heart failure. The ability of Velneperit to modulate peptide levels makes it a candidate for these applications, although clinical trials are necessary to fully understand its efficacy and safety.
Research and Development
Research on Velneperit has included preclinical studies and early-phase clinical trials. These studies aim to evaluate the pharmacokinetics, pharmacodynamics, and therapeutic potential of the compound. Results from these studies will determine the future development of Velneperit as a therapeutic agent.
Related Pages
References
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