Luteoforol: Difference between revisions

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'''Luteoforol''' is a [[chemical compound]] that belongs to the class of [[organic compounds]] known as [[flavonoids]]. Flavonoids are a diverse group of phytonutrients (plant chemicals) found in almost all fruits and vegetables. Luteoforol is specifically classified as a [[flavonol]], a type of flavonoid that has a 3-hydroxyflavone backbone.
{{DISPLAYTITLE:Luteoforol}}


==Chemical Structure==
== Luteoforol ==
The chemical structure of Luteoforol consists of a [[chromen-4-one]] moiety attached to a [[phenyl]] group at the 2-position. The chromen-4-one moiety is a heterocyclic compound that consists of a benzene ring fused to a 1,4-dihydropyran ring. The phenyl group is a cyclic group of atoms with the formula C6H5.
[[File:Luteoforol.svg|thumb|right|Chemical structure of luteoforol]]
'''Luteoforol''' is a type of [[flavan-4-ol]], a class of [[flavonoids]] that are naturally occurring compounds found in various plants. Flavonoids are known for their diverse biological activities and are important in plant pigmentation, UV filtration, symbiotic nitrogen fixation, and as chemical messengers.


==Properties==
== Chemical Structure ==
Luteoforol is a yellow crystalline solid at room temperature. It is soluble in [[ethanol]] and [[dimethyl sulfoxide]] (DMSO), but insoluble in water. The compound has a melting point of 256-258 degrees Celsius.
Luteoforol is characterized by its specific chemical structure, which includes a flavan backbone with a hydroxyl group at the 4-position. The structure of luteoforol can be represented by the chemical formula C15H12O5. The presence of multiple hydroxyl groups contributes to its antioxidant properties.


==Biological Activity==
== Biological Role ==
Luteoforol has been studied for its potential biological activities. Some studies suggest that it may have [[antioxidant]] properties, which means it can neutralize harmful free radicals in the body. Other studies indicate that it may have [[anti-inflammatory]] effects, which could potentially be useful in the treatment of conditions such as arthritis or asthma.
Luteoforol, like other flavonoids, plays a significant role in plant physiology. It is involved in the protection of plants against pathogens and environmental stressors. Additionally, luteoforol contributes to the coloration of flowers and fruits, which is important for attracting pollinators.


==Sources==
== Health Implications ==
Luteoforol is found in various plants, including the [[Sophora japonica]] tree, also known as the Japanese pagoda tree. It can be extracted from the tree's flowers and leaves.
Flavonoids, including luteoforol, are studied for their potential health benefits in humans. They are known for their [[antioxidant]] properties, which help in neutralizing free radicals and reducing oxidative stress. This can potentially lower the risk of chronic diseases such as [[cardiovascular disease]] and certain types of [[cancer]].


==See Also==
== Synthesis and Sources ==
Luteoforol is synthesized in plants through the [[phenylpropanoid pathway]], which is a major metabolic route for the production of flavonoids. It can be found in various plant sources, including fruits, vegetables, and certain herbs. The concentration of luteoforol in plants can vary depending on environmental conditions and the plant species.
 
== Related Compounds ==
Luteoforol is related to other flavonoids such as [[quercetin]], [[kaempferol]], and [[catechin]]. These compounds share similar biosynthetic pathways and biological activities.
 
== Related Pages ==
* [[Flavonoid]]
* [[Flavonoid]]
* [[Flavonol]]
* [[Antioxidant]]
* [[Sophora japonica]]
* [[Phenylpropanoid pathway]]
* [[Cardiovascular disease]]


[[Category:Flavonoids]]
[[Category:Flavonoids]]
[[Category:Phytochemicals]]
[[Category:Antioxidants]]
[[Category:Organic compounds]]
{{Chemistry-stub}}

Latest revision as of 03:38, 13 February 2025


Luteoforol[edit]

Chemical structure of luteoforol

Luteoforol is a type of flavan-4-ol, a class of flavonoids that are naturally occurring compounds found in various plants. Flavonoids are known for their diverse biological activities and are important in plant pigmentation, UV filtration, symbiotic nitrogen fixation, and as chemical messengers.

Chemical Structure[edit]

Luteoforol is characterized by its specific chemical structure, which includes a flavan backbone with a hydroxyl group at the 4-position. The structure of luteoforol can be represented by the chemical formula C15H12O5. The presence of multiple hydroxyl groups contributes to its antioxidant properties.

Biological Role[edit]

Luteoforol, like other flavonoids, plays a significant role in plant physiology. It is involved in the protection of plants against pathogens and environmental stressors. Additionally, luteoforol contributes to the coloration of flowers and fruits, which is important for attracting pollinators.

Health Implications[edit]

Flavonoids, including luteoforol, are studied for their potential health benefits in humans. They are known for their antioxidant properties, which help in neutralizing free radicals and reducing oxidative stress. This can potentially lower the risk of chronic diseases such as cardiovascular disease and certain types of cancer.

Synthesis and Sources[edit]

Luteoforol is synthesized in plants through the phenylpropanoid pathway, which is a major metabolic route for the production of flavonoids. It can be found in various plant sources, including fruits, vegetables, and certain herbs. The concentration of luteoforol in plants can vary depending on environmental conditions and the plant species.

Related Compounds[edit]

Luteoforol is related to other flavonoids such as quercetin, kaempferol, and catechin. These compounds share similar biosynthetic pathways and biological activities.

Related Pages[edit]