Fumarranol: Difference between revisions

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'''Fumarranol''' is a [[natural product]] derived from the [[Fumaria]] genus of plants, specifically [[Fumaria officinalis]]. It is a type of [[alkaloid]] that has been studied for its potential [[pharmacological]] properties.
== Fumarranol ==


==Chemical Structure==
[[File:Fumarranol_structure.png|thumb|right|Chemical structure of Fumarranol]]
Fumarranol is a [[quinolizidine]] alkaloid, meaning it contains a quinolizidine ring in its structure. This ring is a key feature of many alkaloids and is responsible for their biological activity. The exact structure of fumarranol is complex and includes several other functional groups, including a [[hydroxyl]] group and a [[methoxy]] group.


==Pharmacological Properties==
'''Fumarranol''' is a chemical compound that is structurally related to [[fumaric acid]]. It is a derivative of [[fumarate]], which is an important intermediate in the [[citric acid cycle]] (also known as the Krebs cycle or TCA cycle). Fumarranol has been studied for its potential biological activities and its role in various biochemical pathways.
Research into the pharmacological properties of fumarranol is ongoing. Preliminary studies suggest that it may have [[anti-inflammatory]] and [[antioxidant]] properties. It has also been investigated for potential [[anti-cancer]] activity. However, these findings are preliminary and further research is needed to confirm them and to understand the mechanisms of action.


==Toxicity==
== Chemical Structure ==
Like many alkaloids, fumarranol can be toxic in high doses. Symptoms of toxicity can include [[nausea]], [[vomiting]], and [[diarrhea]]. In severe cases, it can cause [[liver damage]] or [[kidney damage]]. Therefore, it should be used with caution and under the supervision of a healthcare professional.


==Sources==
Fumarranol is characterized by its unique chemical structure, which includes a core similar to that of fumaric acid but with additional functional groups that modify its properties. The structure of fumarranol can be visualized in the adjacent image, which shows the arrangement of atoms and the specific functional groups present in the molecule.
Fumarranol is found in the Fumaria genus of plants, particularly Fumaria officinalis. This plant is native to Europe and Asia and has been used in traditional medicine for centuries. It is also cultivated for its ornamental value.


==See Also==
== Biological Significance ==
* [[Alkaloid]]
* [[Fumaria officinalis]]
* [[Pharmacology]]
* [[Toxicity]]


==References==
Fumarranol, like other fumarate derivatives, plays a role in cellular metabolism. It is involved in the [[citric acid cycle]], where it participates in the conversion of [[succinate]] to [[malate]]. This process is crucial for the production of [[adenosine triphosphate]] (ATP), the energy currency of the cell.
<references />


[[Category:Alkaloids]]
== Potential Applications ==
[[Category:Natural products]]
[[Category:Pharmacology]]
[[Category:Toxicology]]


{{pharmacology-stub}}
Research into fumarranol has explored its potential applications in medicine and biochemistry. Due to its structural similarity to fumaric acid, fumarranol may have implications in the treatment of certain metabolic disorders. Additionally, its role in the citric acid cycle makes it a compound of interest in studies of cellular respiration and energy production.
 
== Related Compounds ==
 
Fumarranol is related to several other compounds in the fumarate family, including:
 
* [[Fumaric acid]]
* [[Dimethyl fumarate]]
* [[Fumarate]]
 
These compounds share similar chemical properties and biological functions, making them important subjects of study in biochemistry and pharmacology.
 
== Related Pages ==
 
* [[Citric acid cycle]]
* [[Fumaric acid]]
* [[Metabolism]]
* [[Biochemistry]]
 
[[Category:Biochemistry]]
[[Category:Organic compounds]]

Latest revision as of 11:35, 15 February 2025

Fumarranol[edit]

Chemical structure of Fumarranol

Fumarranol is a chemical compound that is structurally related to fumaric acid. It is a derivative of fumarate, which is an important intermediate in the citric acid cycle (also known as the Krebs cycle or TCA cycle). Fumarranol has been studied for its potential biological activities and its role in various biochemical pathways.

Chemical Structure[edit]

Fumarranol is characterized by its unique chemical structure, which includes a core similar to that of fumaric acid but with additional functional groups that modify its properties. The structure of fumarranol can be visualized in the adjacent image, which shows the arrangement of atoms and the specific functional groups present in the molecule.

Biological Significance[edit]

Fumarranol, like other fumarate derivatives, plays a role in cellular metabolism. It is involved in the citric acid cycle, where it participates in the conversion of succinate to malate. This process is crucial for the production of adenosine triphosphate (ATP), the energy currency of the cell.

Potential Applications[edit]

Research into fumarranol has explored its potential applications in medicine and biochemistry. Due to its structural similarity to fumaric acid, fumarranol may have implications in the treatment of certain metabolic disorders. Additionally, its role in the citric acid cycle makes it a compound of interest in studies of cellular respiration and energy production.

Related Compounds[edit]

Fumarranol is related to several other compounds in the fumarate family, including:

These compounds share similar chemical properties and biological functions, making them important subjects of study in biochemistry and pharmacology.

Related Pages[edit]