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Isoflavan

Lampe JW, Skor HE, Li S et al. Wheat bran and soy protein do not alter urinary excretion of the isoflavan equol in premonopausal women. J. Nutr. 131, 740-744, 2001. [Pg.390]

Kamnaing, P. et al., An isoflavan-quinone and a flavonol from Millettia laurentii. Phytochemistry, 51, 829, 1999. [Pg.730]

Alvarez, L. et al.. Cytotoxic isoflavans from Eysenhardtia polystachya. Journal of Natural Products, 61, 767, 1998. [Pg.1185]

Barragan-Huerta, B.E. et al., Neocandenatone, an isoflavan-cinnamylphenol quinone methide pigment from Dalbergia congestiflora. Phytochemistry, 65, 925, 2004. [Pg.1185]

El-Sebakhy, N.A.A. et al., Antimicrobial isoflavans from Astragalus species. Phytochemistry, 36, 1387, 1994. [Pg.1187]

Fukai, T. et al.. Phenolic constituents of Glycyrrhiza species. 17. Three isoprenoid-substituted isoflavans, gancaonins X-Z, from Chinese folk medicine Tiexin Gancao (root xylems of Glycyrrhiza species). Natural Medicines, 48, 203, 2004. [Pg.1187]

Kinoshita, T. et al., Isoflavan derivatives from Glycyrrhiza glabra (licorice). Heterocycles, 43, 581, 1996. [Pg.1189]

Song, C. et al., Pterocarpans and isoflavans from Astragalus membranaceus bunge, Zhiwu Xuebao, 39, 1169, 1997. [Pg.1194]

Subarnas, A., Oshima, Y., and Hikino, H., Isoflavans and a pterocarpan from Astragalus mongholicus, Phytochemistry, 30, 2777, 1991. [Pg.1194]

Zeng, J.-F. et al., Three prenylated isoflavans from Maackia tenuifolia. Phytochemistry, 47, 903, 1998. [Pg.1197]

Zeng, J.-F., Tan, C.-H., and Zhu, D.-Y., Manuifolin Q, an unusual 4-aryl-substituted isoflavan from Maackia tenuifolia, Journal of Asian Natural Products Research, 6, 45, 2004. [Pg.1197]

Many flavonoids are known to be phytoalexins, antiviral agents, and to serve as antiinflammatory and antitumor compounds. Several isoflavones have estrogenic activity in mammals (70). (-)-Vestitol and sativan, isoflavans from Lotus species, are phytoalexins. 3R(-)-Vestitol from the resistant pasture legume Lotus pedunculatus, has been demonstrated to be a feeding deterrent... [Pg.316]

The difference of the substituents at C-5 is expected that European and Chinese licorices exhibit different actions in therapeutically use. For example, 5,6-disubstituted isoflavans do not showed a potency of... [Pg.206]


See other pages where Isoflavan is mentioned: [Pg.677]    [Pg.164]    [Pg.60]    [Pg.21]    [Pg.116]    [Pg.375]    [Pg.416]    [Pg.566]    [Pg.1101]    [Pg.1102]    [Pg.1129]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1130]    [Pg.1135]    [Pg.1190]    [Pg.1192]    [Pg.1192]    [Pg.1194]    [Pg.1194]    [Pg.206]    [Pg.206]    [Pg.207]   
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See also in sourсe #XX -- [ Pg.31 , Pg.32 ]

See also in sourсe #XX -- [ Pg.4 , Pg.388 , Pg.389 , Pg.391 , Pg.392 ]

See also in sourсe #XX -- [ Pg.4 , Pg.388 , Pg.389 , Pg.391 , Pg.392 ]

See also in sourсe #XX -- [ Pg.232 ]




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Isoflavan derivatives

Isoflavanones Isoflavans

Isoflavans

Isoflavans

Isoflavans synthesis

Isoflavans via isoflavones

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