4-Caffeoyl-1,5-quinide

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4-Caffeoyl-1,5-quinide.svg

Chemical compound


4-Caffeoyl-1,5-quinide
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Chemical formula CHNO
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4-Caffeoyl-1,5-quinide is a chemical compound that belongs to the class of quinides. It is a derivative of caffeic acid and is structurally related to chlorogenic acid. This compound is of interest in the field of phytochemistry and has been studied for its potential biological activity.

Structure and Properties[edit | edit source]

4-Caffeoyl-1,5-quinide is characterized by the presence of a caffeoyl group attached to a quinide structure. The molecular structure includes a phenolic ring, which is responsible for its antioxidant properties. The compound is typically studied using techniques such as NMR spectroscopy, mass spectrometry, and chromatography.

Sources[edit | edit source]

This compound can be found in various plant species, particularly those that are rich in phenolic compounds. It is often identified in the context of coffee research, as it is a derivative of compounds found in coffee beans.

Biological Activity[edit | edit source]

Research has indicated that 4-Caffeoyl-1,5-quinide may exhibit several biological activities, including antioxidant, anti-inflammatory, and antimicrobial effects. These properties make it a compound of interest for potential therapeutic applications.

Synthesis[edit | edit source]

The synthesis of 4-Caffeoyl-1,5-quinide can be achieved through various chemical reactions involving caffeic acid and related compounds. The process typically involves esterification and cyclization reactions.

Applications[edit | edit source]

Due to its potential biological activity, 4-Caffeoyl-1,5-quinide is studied for its possible use in pharmaceuticals, nutraceuticals, and cosmetics. Its antioxidant properties are particularly valued in the development of products aimed at reducing oxidative stress.

See also[edit | edit source]

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD