Showing posts with label anthocyanidins. Show all posts
Showing posts with label anthocyanidins. Show all posts

Saturday, December 30, 2023

Anthocyanidins: Health-Promoting Natural Compounds

Anthocyanidins, free of sugar, function as counterparts to anthocyanins and are built upon the benzopyrylium (chromenylium) ion. Specifically, they constitute salt derivatives of the 2-phenylchromenylium cation, commonly known as the flavylium cation, with chloride primarily serving as the counterion.

Distinguishing themselves from other flavonoids owing to their positive charge, anthocyanidins achieve stability through the incorporation of a glycose moiety, typically glucose, at the 3-position. This glycosylation process is facilitated by flavonoid 3-glucosyltransferase (GT). Anthocyanidins can be classified into 3-hydroxyanthocyanidins, 3-deoxyanthocyanidins, and O-methylated anthocyanidins.

Nature harbors around 17 anthocyanidins, with six—cyanidin, delphinidin, petunidin, peonidin, pelargonidin, and malvidin, where cyanidin is the predominant one—being widely distributed and holding substantial importance for humans. Apart from their role as natural dyes, anthocyanidins showcase pharmaceutical potential, presenting various health benefits.

Scientific inquiries, spanning cell culture studies, animal models, and human clinical trials, confirm the antioxidative and antimicrobial attributes of anthocyanidins. These compounds contribute to improved visual and neurological health and offer protection against a range of non-communicable diseases.
Anthocyanidins: Health-Promoting Natural Compounds

Tuesday, September 24, 2019

Anthocyanidins

Anthocyanidins are the sugar-free counterparts of anthocyanins based on the benzopyrylium (chromenylium) ion. In particular anthocyanidins are salt derivatives of the 2-phenylchromenylium cation, also known as flavylium cation. The counterion of the flavylium cation is mostly chloride.

With this positive charge, the anthocyanidins differ from other flavonoids. Anthocyanidins are stabilized with addition of glycose moiety, usually glucose moiety, at the 3-position of the anthocyanidin in a reaction catalyzed by flavonoid 3-glucosyltrasferase (GT). Anthocyanidins are grouped into 3-hydroxyanthocyanidins, 3-deoxyanthocyanidins, and O-methylated anthocyanidins.

There are about 17 anthocyanidins found in nature, but only six (cyanidin, delphinidin, petunidin, peonidin, pelargonidin, and malvidin, with cyanidin being the most common) are ubiquitously spread and of great importance in human. Besides the use of anthocyanidins as natural dyes, these colored pigments are potential pharmaceutical ingredients that give various beneficial health effects.

Scientific studies, such as cell culture studies, animal models, and human clinical trials, show that anthocyanidins possess antioxidative and antimicrobial activities, improve visual and neurological health, and protect against various non-communicable diseases.
Anthocyanidins

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