Chromone

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Chromone[edit | edit source]

Chemical structure of Chromone

Chromone is a heterocyclic organic compound with the molecular formula C9H6O2. It is a derivative of benzopyran and is composed of a benzene ring fused to a pyran ring. Chromone is known for its diverse range of biological activities and is widely studied for its potential therapeutic applications.

History[edit | edit source]

Chromone was first synthesized in 1884 by the German chemist Hermann von Pechmann. He obtained it by heating salicylaldehyde with zinc acetate. Since then, chromone and its derivatives have attracted significant attention from researchers due to their interesting chemical properties and biological activities.

Chemical Properties[edit | edit source]

Chromone possesses a unique chemical structure that consists of a benzene ring fused to a pyran ring. This structure imparts several important properties to chromone, including its ability to act as a versatile scaffold for the synthesis of various compounds. The presence of different functional groups on the chromone molecule allows for modifications that can enhance its biological activity.

Biological Activities[edit | edit source]

Chromone and its derivatives have been extensively studied for their diverse range of biological activities. They have shown promising results in various therapeutic areas, including anti-inflammatory, antioxidant, anticancer, antimicrobial, and antiviral activities. These properties make chromone an attractive candidate for the development of new drugs.

Applications[edit | edit source]

Due to its wide range of biological activities, chromone has found applications in various fields. In the pharmaceutical industry, chromone derivatives are being explored as potential drug candidates for the treatment of diseases such as cancer, inflammation, and viral infections. Additionally, chromone-based compounds have also been used as fluorescent probes in biological imaging studies.

References[edit | edit source]


See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD