Luteoforol
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.
Chemical Structure[edit | edit source]
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.
Properties[edit | edit source]
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.
Biological Activity[edit | edit source]
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.
Sources[edit | edit source]
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.
See Also[edit | edit source]
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Contributors: Prab R. Tumpati, MD