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・ Anthocharis sara
・ Anthocharis sara thoosa
・ Anthocharis scolymus
・ Anthocharis stella
・ Anthocharis stella browningi
・ Anthochori
・ Anthochori, Arcadia
・ Anthochori, Kozani
・ Anthochortus
・ Anthocleista
・ Anthocleista grandiflora
・ Anthocleista microphylla
・ Anthocleista scandens
・ Anthocoridae
・ Anthocoris
Anthocyanidin
・ Anthocyanidin 3-O-glucosyltransferase
・ Anthocyanidin reductase
・ Anthocyanin
・ Anthocyanin 3'-O-beta-glucosyltransferase
・ Anthocyanin 3-O-glucoside 6''-O-hydroxycinnamoyltransferase
・ Anthocyanin 5-aromatic acyltransferase
・ Anthocyanin 5-O-glucoside 6'''-O-malonyltransferase
・ Anthocyanin 5-O-glucosyltransferase
・ Anthocyanin 6"-O-malonyltransferase
・ Anthocyanone A
・ Anthodes
・ Anthodiscus
・ Anthodiscus chocoensis
・ Anthodiscus montanus


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Anthocyanidin : ウィキペディア英語版
Anthocyanidin

Anthocyanidins are common plant pigments. They are the sugar-free counterparts of anthocyanins based on the flavylium ion or 2-phenylchromenylium, which is a type of oxonium ion (chromenylium is referred also to as benzopyrylium).〔(IUPAC Goldbook )〕 They form a large group of polymethine dye. In particular anthocyanidins are salt derivatives of the 2-phenylchromenylium cation, also known as flavylium cation. As shown in the figure below, the phenyl group at the 2-position can carry different substituents. The counterion of the flavylium cation is mostly chloride. With this positive charge, the anthocyanidins differ from other flavonoids.
== pH ==
The stability of anthocyanidins is dependent on pH. At a low pH (acidic conditions), colored anthocyanidins are present, whereas at a higher pH (basic conditions) the colorless chalcones forms are present.



抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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