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Rutinosides

Chemical Neme 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1 -benzopyran-4-one-7-rutinoside... [Pg.510]

Several complexes of [Bu2Sn(IV)] with flavonoid glycosides 3-[6-0-(6-deoxy-a-L-mannopyranosyl)-(jS-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-H-l-benzopyran-4-one (rutin) and 2, 4, 3-trihydroxy-5, 4-dimetoxychalcone 4-rutinoside (hesperidin) and flavonoid aglycones (quercetin, morin, hesperitin, and other flavones) (Figure 5) were prepared. [Pg.377]

The effects of pH under model conditions (0.6 to 5.5 for 24 hr) were covered by Nielsen et al. for four anthocyanins (3-O-glucoside, glycosylated cyanidin, rutinoside, and delphinidin rutinoside). After 24 hr, over 90% of the anthocyanins were intact up to pH 3.3, while instabihty greatly increased at pH greater than 4.5. [Pg.72]

Wu, X., Cao, G., and Prior, R.L., Absorption and metabolism of anthocyanins in elderly women after consumption of elderberry or blueberry, J. Nutr, 132,1865, 2002. Matsumoto, H. et al.. Orally administered delphinidin 3-rutinoside and cyanidin 3-rutinoside are directly absorbed in rats and humans and appear in the blood as the intact forms, J. Agric. Food Chem., 49, 1546, 2001. [Pg.174]

Cyanidin 3-glucoside and cyanidin 3-rutinoside were degraded at 100°C in weak acidic solutions at pH range 1 to 4 under aerobic and anaerobic conditions." The degradation revealed that cyanidin 3-glucoside was more stable under both conditions." ... [Pg.261]

Adams, J.B. and Woodman, J.S., Thermal degradation of anthocyanins with particular reference to the 3-glucosides of cyanidin. 2 - Anaerobic degradation of cyanidin-3-rutinoside at 100°C and pH 3.0 in presence of sodium sulfite, J. Sci. Food Agric., 24, 763, 1973. [Pg.275]

The plant is known elaborate a series of quite unusual phenanthrene alkaloid derivatives, of which aristoliukine-C, aristofolin A and E, aristolochic acid-la methyl ester, and aristolochic acid. Other chemical constituents found in this plant are flavonoid glycosides such as kaempferol-3-O-rutinoside and quercetin kaempferol-3-O-rutinoside (3,4). Exposure to Aristolochiaceae family is associated with the development of cancer in humans. A significant advance is the toxicological effects of aristolochic acid has been provided by the work of Pezzuto et al. They showed that aristolochic acid is a mutagen... [Pg.20]


See other pages where Rutinosides is mentioned: [Pg.378]    [Pg.277]    [Pg.277]    [Pg.279]    [Pg.6]    [Pg.66]    [Pg.67]    [Pg.83]    [Pg.83]    [Pg.83]    [Pg.84]    [Pg.118]    [Pg.193]    [Pg.194]    [Pg.254]    [Pg.276]    [Pg.276]    [Pg.72]    [Pg.249]    [Pg.255]    [Pg.259]    [Pg.267]    [Pg.494]    [Pg.461]    [Pg.20]    [Pg.26]    [Pg.30]    [Pg.80]    [Pg.313]    [Pg.149]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.243]    [Pg.244]    [Pg.244]    [Pg.262]    [Pg.276]   
See also in sourсe #XX -- [ Pg.67 , Pg.69 , Pg.81 , Pg.84 , Pg.86 ]

See also in sourсe #XX -- [ Pg.95 ]

See also in sourсe #XX -- [ Pg.238 ]




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3-O-rutinosides

3-Rutinoside 5-glucoside

7-Rutinoside

Apigenin 7-O-rutinoside

Apigenin 7-rutinoside

Cyanidin 3-O-rutinoside

Cyanidin-3-rutinoside

Delphinidin-3-O-rutinoside

Delphinidin-3-rutinoside-7 -glucosid

Flavanone rutinosides

Hesperetin 7-O-rutinoside

Hesperetin-7-rutinoside

Hesperidin (3 ,5,7-trihydroxy-4 methoxyflavanone-7-rutinoside

Hesperidin (3 ,5,7-trihydroxy-4 methoxyflavanone-7-rutinoside effects on ACE

Isorhamnetin-3-O-rutinoside

Kaempferol 3-rutinoside

Kaempferol-3-O-rutinoside

Luteolin 7-O-rutinoside

Luteolin-7-rutinoside

Myricetin-3-0-rutinoside from

Myricetin-3-O-rutinoside

Naringenin-7-O-rutinoside

Naringenin-7-rutinoside

Pelargonidin 3-rutinoside

Pelargonidin-3-rutinoside-5-glucosid

Pelargonidin-3-rutinoside-5-glucoside

Peonidin 3-rutinoside

Quercetin 3-rutinoside 4 -diglucosid

Quercetin 3-rutinoside 4 -diglucoside

Quercetin-3-0-rutinoside

Quercetin-3-O-rutinoside

Quercitrin-3-rutinoside

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