Nitroxyl: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
Line 1: Line 1:
'''Nitroxyl''' (also known as '''HNO''') is a reactive nitrogen species that is a powerful reducing agent. It is the one-electron reduction product of nitric oxide (NO) and is isoelectronic with dioxygen. Nitroxyl can be formed from the reduction of nitric oxide or from the protonation of nitroxide (NO−). Nitroxyl is a powerful reducing agent, and it reacts with oxygen to form nitric oxide and water.
{{Short description|Overview of Nitroxyl in medical and biochemical contexts}}


==Chemistry==
==Nitroxyl==
Nitroxyl is a reactive nitrogen species that is a powerful reducing agent. It is the one-electron reduction product of nitric oxide (NO) and is isoelectronic with dioxygen. Nitroxyl can be formed from the reduction of nitric oxide or from the protonation of nitroxide (NO−). Nitroxyl is a powerful reducing agent, and it reacts with oxygen to form nitric oxide and water.
Nitroxyl, also known as azanone, is the chemical compound with the formula HNO. It is the one-electron reduced and protonated form of nitric oxide (NO), and it plays a significant role in various biological processes. Nitroxyl is a reactive nitrogen species that has been studied for its potential therapeutic applications, particularly in cardiovascular medicine.


==Biological role==
==Chemical Properties==
In biological systems, nitroxyl has been found to have a number of important roles. It is involved in the regulation of vascular tone, neurotransmission, and immune response. Nitroxyl can also react with a number of biological targets, including thiols, metals, and nucleophiles.
Nitroxyl is a highly reactive molecule that exists in equilibrium with its dimer, hyponitrous acid (H_N_O_). It is a transient species that can be generated in situ from various precursors, such as Angeli's salt or Piloty's acid. Due to its reactivity, nitroxyl is challenging to study directly, and its effects are often inferred from the behavior of its precursors or reaction products.


==Medical applications==
==Biological Significance==
Due to its biological activity, nitroxyl has potential applications in medicine. It has been shown to have vasodilatory effects, and it may have potential as a treatment for heart failure. Nitroxyl donors have also been investigated for their potential as anticancer agents.
Nitroxyl has been shown to have distinct biological effects compared to nitric oxide. It can interact with thiols and metal centers in proteins, leading to various physiological responses. One of the most notable effects of nitroxyl is its ability to induce vasodilation, which is the widening of blood vessels. This property makes it a molecule of interest in the treatment of heart failure and other cardiovascular diseases.


==See also==
===Cardiovascular Effects===
Nitroxyl donors have been investigated for their potential to improve cardiac function. Unlike nitric oxide, which primarily activates soluble guanylate cyclase (sGC) to increase cyclic GMP levels, nitroxyl can also directly modify thiol groups on proteins, leading to enhanced cardiac contractility and vasodilation. This dual mechanism of action suggests that nitroxyl could be beneficial in conditions where nitric oxide signaling is impaired.
 
===Antioxidant Properties===
Nitroxyl is also known for its antioxidant properties. It can scavenge reactive oxygen species (ROS) and protect cells from oxidative stress. This activity contributes to its potential therapeutic benefits in diseases characterized by excessive oxidative damage.
 
==Synthesis and Detection==
Due to its instability, nitroxyl is typically generated from chemical precursors. Angeli's salt (Na_N_O_) is a commonly used nitroxyl donor that releases HNO upon decomposition. Detection of nitroxyl in biological systems is challenging, but it can be inferred through the use of specific probes or by monitoring the effects of known nitroxyl donors.
 
==Potential Therapeutic Applications==
Research into nitroxyl has highlighted its potential as a therapeutic agent in several areas:
 
* '''Heart Failure:''' Nitroxyl donors have shown promise in preclinical models of heart failure, improving cardiac output and reducing symptoms.
* '''Hypertension:''' By inducing vasodilation, nitroxyl could help lower blood pressure in hypertensive patients.
* '''Neuroprotection:''' The antioxidant properties of nitroxyl may offer neuroprotective benefits in conditions such as stroke or neurodegenerative diseases.
 
==Challenges and Future Directions==
Despite its potential, the clinical application of nitroxyl is limited by challenges in its delivery and stability. Ongoing research aims to develop more stable nitroxyl donors and to better understand the molecular mechanisms underlying its effects. Future studies will focus on optimizing nitroxyl-based therapies for clinical use.
 
==Related Pages==
* [[Nitric oxide]]
* [[Nitric oxide]]
* [[Reactive nitrogen species]]
* [[Reactive nitrogen species]]
* [[Nitroxide]]
* [[Vasodilation]]
 
* [[Heart failure]]
[[Category:Chemical compounds]]
* [[Oxidative stress]]
[[Category:Reactive nitrogen species]]
[[Category:Medical applications]]
 
{{stub}}


= Nitroxyl Azanon =
[[Category:Biochemistry]]
<gallery>
[[Category:Cardiovascular pharmacology]]
File:Nitroxyl Azanon.svg|Nitroxyl Azanon structure
[[Category:Nitrogen compounds]]
File:Nitrosocyclohexyl_acetate.png|Nitrosocyclohexyl acetate structure
</gallery>

Revision as of 17:44, 18 February 2025

Overview of Nitroxyl in medical and biochemical contexts


Nitroxyl

Nitroxyl, also known as azanone, is the chemical compound with the formula HNO. It is the one-electron reduced and protonated form of nitric oxide (NO), and it plays a significant role in various biological processes. Nitroxyl is a reactive nitrogen species that has been studied for its potential therapeutic applications, particularly in cardiovascular medicine.

Chemical Properties

Nitroxyl is a highly reactive molecule that exists in equilibrium with its dimer, hyponitrous acid (H_N_O_). It is a transient species that can be generated in situ from various precursors, such as Angeli's salt or Piloty's acid. Due to its reactivity, nitroxyl is challenging to study directly, and its effects are often inferred from the behavior of its precursors or reaction products.

Biological Significance

Nitroxyl has been shown to have distinct biological effects compared to nitric oxide. It can interact with thiols and metal centers in proteins, leading to various physiological responses. One of the most notable effects of nitroxyl is its ability to induce vasodilation, which is the widening of blood vessels. This property makes it a molecule of interest in the treatment of heart failure and other cardiovascular diseases.

Cardiovascular Effects

Nitroxyl donors have been investigated for their potential to improve cardiac function. Unlike nitric oxide, which primarily activates soluble guanylate cyclase (sGC) to increase cyclic GMP levels, nitroxyl can also directly modify thiol groups on proteins, leading to enhanced cardiac contractility and vasodilation. This dual mechanism of action suggests that nitroxyl could be beneficial in conditions where nitric oxide signaling is impaired.

Antioxidant Properties

Nitroxyl is also known for its antioxidant properties. It can scavenge reactive oxygen species (ROS) and protect cells from oxidative stress. This activity contributes to its potential therapeutic benefits in diseases characterized by excessive oxidative damage.

Synthesis and Detection

Due to its instability, nitroxyl is typically generated from chemical precursors. Angeli's salt (Na_N_O_) is a commonly used nitroxyl donor that releases HNO upon decomposition. Detection of nitroxyl in biological systems is challenging, but it can be inferred through the use of specific probes or by monitoring the effects of known nitroxyl donors.

Potential Therapeutic Applications

Research into nitroxyl has highlighted its potential as a therapeutic agent in several areas:

  • Heart Failure: Nitroxyl donors have shown promise in preclinical models of heart failure, improving cardiac output and reducing symptoms.
  • Hypertension: By inducing vasodilation, nitroxyl could help lower blood pressure in hypertensive patients.
  • Neuroprotection: The antioxidant properties of nitroxyl may offer neuroprotective benefits in conditions such as stroke or neurodegenerative diseases.

Challenges and Future Directions

Despite its potential, the clinical application of nitroxyl is limited by challenges in its delivery and stability. Ongoing research aims to develop more stable nitroxyl donors and to better understand the molecular mechanisms underlying its effects. Future studies will focus on optimizing nitroxyl-based therapies for clinical use.

Related Pages