Английская Википедия:Catechin-7-O-glucoside

Материал из Онлайн справочника
Версия от 18:34, 15 февраля 2024; EducationBot (обсуждение | вклад) (Новая страница: «{{Английская Википедия/Панель перехода}} {{DISPLAYTITLE:Catechin-7-''O''-glucoside}} {{Chembox | Name = Catechin-7-''O''-glucoside | ImageFile = Catechin-7-O-glucoside.svg | ImageSize = 300px | ImageAlt = Chemical structure of catechin-7-''O''-glucoside | IUPACName = (2''S'',4''S'',5''S'')-2-<nowiki>[[</nowiki>(2''R'',3''S'')-2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2''H''-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4...»)
(разн.) ← Предыдущая версия | Текущая версия (разн.) | Следующая версия → (разн.)
Перейти к навигацииПерейти к поиску

Шаблон:Chembox

Catechin-7-O-glucoside is a flavan-3-ol glycoside formed from catechin.

Natural occurrences

Catechin-7-O-glucoside can be isolated from the hemolymph of the European pine sawfly (Neodiprion sertifer).[1] It also occurs in relatively large quantities in cowpea (Vigna unguiculata) as the dominant flavan-3-ol monomer, and actually accounts for up to 70% of cowpea proanthocyanidins (tannins).[2]

It can also be produced by biotransformation of (+)-catechin by cultured cells of Eucalyptus perriniana.[3]

Presence in natural traditional drugs

Catechin-7-O-glucoside can be found in paeoniae radix, the crude drug made from the roots of Chinese peony (Paeonia lactiflora),[4] in red knotweed (Bistorta macrophylla, also known as Polygonum macrophyllum),[5] in the stem barks of the Nepali hog plum (Choerospondias axillaris),[6] in the Korean plum yew (Cephalotaxus koreana)[7] and in Huanarpo Macho (Jatropha macrantha).[8] (−)-Catechin 7-O-β-D-glucopyranoside is found in the bark of Rhaphiolepis umbellata.[9]

Presence in food

It is found in buckwheat groats,[10] in the red bean (the seed of Vigna umbellata, formerly known as Phaseolus calcaratus),[11] in barley (Hordeum vulgare L.) and malt.[12] (−)-Catechin 7-O'-β-D-glucopyranoside is found in rhubarb.[9]

Health effects

This compound has an antioxidant activity leading to a cytoprotective effect.[11][13]

References

Шаблон:Reflist

Шаблон:Flavanol