apigenin-7-o-glucuronide and vitexin

apigenin-7-o-glucuronide has been researched along with vitexin* in 1 studies

Other Studies

1 other study(ies) available for apigenin-7-o-glucuronide and vitexin

Article	Year
Chemotaxonomic features associated with flavonoids of cannabinoid-free cannabis (Cannabis sativa subsp. sativa L.) in relation to hops (Humulus lupulus L.). Natural product letters, 2002, Volume: 16, Issue:1 The major flavonoids present in the leaves and flowers of the cannabinoid-free cannabis (Cannabis sativa subsp. sativa L.) cultivars Felina and Futura are orientin (1), vitexin (2), luteolin-7-O-beta-D-glucuronide (3), and apigenin-7-O-beta-D-glucuronide (4), while prenylated flavonoids, to which the potent estrogenicity of hops (Humilus lupulus L.) is associated, are absent. The different composition of flavonoids has chemotaxonomic value. Topics: Apigenin; beta-Glucosidase; Cannabis; Chromatography, High Pressure Liquid; Estrogens; Flavonoids; Glucosides; Glucuronidase; Humans; Humulus; Hydrolysis; Luteolin; Mass Spectrometry; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Leaves; Plants, Medicinal; Receptors, Estrogen; Saccharomyces cerevisiae; Spectrometry, Mass, Electrospray Ionization	2002

Article

Year

Chemotaxonomic features associated with flavonoids of cannabinoid-free cannabis (Cannabis sativa subsp. sativa L.) in relation to hops (Humulus lupulus L.).

Natural product letters, 2002, Volume: 16, Issue:1

The major flavonoids present in the leaves and flowers of the cannabinoid-free cannabis (Cannabis sativa subsp. sativa L.) cultivars Felina and Futura are orientin (1), vitexin (2), luteolin-7-O-beta-D-glucuronide (3), and apigenin-7-O-beta-D-glucuronide (4), while prenylated flavonoids, to which the potent estrogenicity of hops (Humilus lupulus L.) is associated, are absent. The different composition of flavonoids has chemotaxonomic value.

Topics: Apigenin; beta-Glucosidase; Cannabis; Chromatography, High Pressure Liquid; Estrogens; Flavonoids; Glucosides; Glucuronidase; Humans; Humulus; Hydrolysis; Luteolin; Mass Spectrometry; Molecular Structure; Nuclear Magnetic Resonance, Biomolecular; Plant Leaves; Plants, Medicinal; Receptors, Estrogen; Saccharomyces cerevisiae; Spectrometry, Mass, Electrospray Ionization

2002