Example sentences for: isoflavone

How can you use “isoflavone” in a sentence? Here are some example sentences to help you improve your vocabulary:

  • utilis) that produce a dose-related increase in the clotting time of blood induced by carpet viper venom ( Echis carinatus ) would be useful against bites from Bothrops species that cause haemorrhage at the point of injection due to the inhibition of the clotting mechanism [ 40 ] . Antivenom compounds so far isolated from plants include protocatechuic acid, a catechin-gallo-catechin tannin, caffeic acid derivatives (chlorogenic acid, cynarin), coumarins (bergapten), flavonoids (rutin, isoscutellarein, kaempferol, quercetin, hesperidin), ar-turmerone, alkaloids (aristolochic acid), triterpenoids, triterpenes, coumestans (wedelolactone), sterols (sitosterol, stigmasterol, beta-amyrin), triterpenoid glycosides, alkaloids (allantoin) and lignoflavonoids [ 43 40 44 42 ] . Many relevant compounds are widely distributed nitrogen-free, low molecular weight compounds (except aristolochic acid, an untypical non-basic, nitro-derivative) [ 38 ] . The structural similarities of certain plant chemicals found in plants used for snakebites are an isoflavone skeleton, acidic nature and dioxygenated functionality [ 44 ] .

  • The data for this study come from a randomized double-blind study investigating the effects of a 100 mg/day soy isoflavone regimen on estrogen levels in 34 premenopausal women.

  • Intake of soy foods according to the SQ in a validation study among 102 women was highly correlated with urinary isoflavone excretion [ 14].

  • The final assay was carried out as described elsewhere [ 60 61 ] . Equol was determined in the same way genistein and daidzein, using an antiserum to 4'-O-carboxymethyl-equol-bovine serum albumin and the Europium label was synthesized using the same derivative of equol [ 62 ] . The cross-reactivities of the genistein and daidzein antisera with other isoflavone metabolites have been described previously [ 60 ] . The equol antiserum showed a cross reactivity of 0% for genistein, 12% for dihydrogenistein, 4% for dihydrodaidzein and less than 1% for daidzein and its other metabolites.


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