2013
DOI: 10.1177/1934578x1300800511
|View full text |Cite
|
Sign up to set email alerts
|

Antioxidant Activity of the Isoflavonoids from the Roots of Maackia amurensis

Abstract: Seven isoflavonoids, including a new glycoside, (6aR,11aR)-medicarpin-3-O-gentiobioside (6), were isolated from the roots of Maackia amurensis using repeated column chromatography on a Toyopearl HW-50F sorbent and identified by HPLC-PDA-MS, 1 H NMR, 13 C, 1 H-1 H COSY, HSQC NMR and HMBC NMR analyses as daidzin (1), genistein-7-O-gentiobioside (2), pseudobaptigenin-7-O-gentiobioside (3), formononetin-7-O-gentiobioside (4), (6aR,11aR)maackiain-3-O-gentiobioside (5), and 5-O-methylgenistein-7-O-gentiobioside (7).… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
3
0
6

Year Published

2016
2016
2023
2023

Publication Types

Select...
4

Relationship

1
3

Authors

Journals

citations
Cited by 4 publications
(9 citation statements)
references
References 10 publications
0
3
0
6
Order By: Relevance
“…Additionally, the Oglycoside linkage in structures was confirmed, depending on the characteristic down-field location of C-6" at δ 70.37 ppm. Also the presence of doublet at δ 5.39 for the anomeric proton H-1′′′ of the terminal sugar moiety was intrinsic for (1′′′ -6′′) O-glycoside moiety 28 . The assignment of all other 13 C NMR resonances of compound 4 was achieved by comparison with the corresponding data of structural related compounds 9,15,19,22,23 .…”
Section: Characterization and Identification Of Isolated Compoundsmentioning
confidence: 99%
“…Additionally, the Oglycoside linkage in structures was confirmed, depending on the characteristic down-field location of C-6" at δ 70.37 ppm. Also the presence of doublet at δ 5.39 for the anomeric proton H-1′′′ of the terminal sugar moiety was intrinsic for (1′′′ -6′′) O-glycoside moiety 28 . The assignment of all other 13 C NMR resonances of compound 4 was achieved by comparison with the corresponding data of structural related compounds 9,15,19,22,23 .…”
Section: Characterization and Identification Of Isolated Compoundsmentioning
confidence: 99%
“…Äëÿ áîëåå ýôôåêòèâíîãî ïðèìåíåíèÿ óíèêàëüíîãî ðåëèêòîâîãî ðàñòåíèÿ â ôàðìàöåâòè÷åñêîé ïðîìûøëåííîñòè âàaeíî áûëî îöåíèòü âîçìîaeíîñòü èñïîëüçîâàíèÿ äðóãèõ îðãàíîâ ðàñòåíèÿ, íàïðèìåð êîðíåé, â êà÷åñòâå àëüòåðíàòèâíîãî èñòî÷íèêà ñûðüÿ äëÿ ñîçäàíèÿ ôàðìàöåâòè÷åñêèõ ïðåïàðàòîâ. Íåäàâíî ìû ïîêàçàëè, ÷òî êîðíè, â îòëè÷èå îò äðåâåñèíû ðàñòåíèÿ M. amurensis, ñîäåðaeàò ñâûøå 78 % ãëèêîçèäíûõ ôîðì èçîôëàâîíîâ è ïòåðîêàðïàíîâ [12,13]. Ïðè ýòîì êîìïëåêñ èçîôëàâîíîèäîâ èç êîðíåé M. amurensis îáëàäàåò âûðàaeåííûìè àíòèîêñèäàíòíûìè [13] è ãåïàòîïðîòåêòèâíûìè ñâîéñòâàìè [12 -15] è ÿâëÿåòñÿ ïåðñïåêòèâíûì äëÿ ñîçäàíèÿ íîâûõ ôàðìàöåâòè÷åñêèõ ñðåäñòâ íà åãî îñíîâå.…”
Section: ðàñòåíèå ìààêèÿ àìóðñêàÿ (Maackia Amurensisunclassified
“…Íåäàâíî ìû ïîêàçàëè, ÷òî êîðíè, â îòëè÷èå îò äðåâåñèíû ðàñòåíèÿ M. amurensis, ñîäåðaeàò ñâûøå 78 % ãëèêîçèäíûõ ôîðì èçîôëàâîíîâ è ïòåðîêàðïàíîâ [12,13]. Ïðè ýòîì êîìïëåêñ èçîôëàâîíîèäîâ èç êîðíåé M. amurensis îáëàäàåò âûðàaeåííûìè àíòèîêñèäàíòíûìè [13] è ãåïàòîïðîòåêòèâíûìè ñâîéñòâàìè [12 -15] è ÿâëÿåòñÿ ïåðñïåêòèâíûì äëÿ ñîçäàíèÿ íîâûõ ôàðìàöåâòè÷åñêèõ ñðåäñòâ íà åãî îñíîâå. Öåëüþ íàñòîÿùåé ðàáîòû ÿâèëîñü äåòàëüíîå èññëåäîâàíèå õèìè÷åñêîãî ñîñòàâà âûäåëåííîãî èç ýêñòðàêòà êîðíåé ìààêèè àìóðñêîé êîìïëåêñà èçîôëàâîíîèäîâ è èçó÷åíèå åãî âëèÿíèÿ íà ñîñòîÿíèå óãëåâîäíîãî îáìåíà ïå÷åíè êðûñ â óñëîâèÿõ èíòîêñèêàöèè ÷åòûðåõõëîðèñòûì óãëåðîäîì.…”
Section: ðàñòåíèå ìààêèÿ àìóðñêàÿ (Maackia Amurensisunclassified
See 2 more Smart Citations