ライフサイエンスコーパス: biochanin A

コーパス検索結果 (１語後でソート)

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1 fate, genistein 7-sulfate, or genistein from biochanin A.

2 cubated with [4-(14)C]genistein and [4-(14)C]biochanin A.

3 cell lines by the isoflavones genistein and biochanin A.

4 Glucosides of biochanin A (4'-O-methylgenistein) and pratensein (3'-hy

5 orogenic acid (15.4 +/- 0.05 mug mg(-1)) and biochanin A (9.6 +/- 0.06 mug GAE mg(-1)), while minor c

6 ein, genistein, glycitein, formononetin, and biochanin-A and their mammalian metabolites equol and O-

7 flavonoids, isoflavonoids (formononetin and biochanin A) and flavones (7,4'-dihydroxyflavone), respe

8 flavones (genistein, genistin, daidzein, and biochanin A) and soy phytochemical concentrate exhibit d

9 isoflavones (genistein, daidzein, glycitein, biochanin A, and formononetin), lignans (secoisolaricire

10 ding the flavonol kaempferol, the isoflavone biochanin A, and the chalcone isoliquiritigenin.

11 ch are aglycons, namely daidzein, genistein, biochanin A, and two of which, daidzin and genistin, are

12 oybean isoflavones (genistein, daidzein, and biochanin A) are ERbeta-selective agonists of transcript

13 From a panel of phytoestrogen isoflavones, biochanin A (BCA) was identified as the most potent indu

14 n (genistein 7-sulfate) and 2 metabolites of biochanin A (genistein and genistein 7-sulfate) were det

15 Environmental half-lives for biochanin A, genistein, and equol are expected to vary o

16 Biochanin A, genistein, and equol degraded relatively sl

17 s of the isoflavones daidzein, formononetin, biochanin A, genistein, and equol were studied under sim

18 n, isoformononetin glycoside and malonylated biochanin A glycoside the major compounds.

19 timulated release of PSA, presumably because biochanin A increased UDPGT and increased the intracellu

20 Additionally, biochanin A markedly decreased prostate specific antigen

21 Intact cells treated with biochanin A produced testosterone-glucuronide from testo

22 Biochanin A significantly decreased the testosterone-sti

23 nap2 mutants and show that the phytoestrogen biochanin A specifically reverses the mutant behavioral

24 f genistein 7-sulfate from genistein or with biochanin A sulfate, genistein 7-sulfate, or genistein f

25 ted methylated form of each isoflavone and a biochanin A sulfate.

26 avonoid metabolites such as formononetin and biochanin-A that peaked at 12 to 18 h following elicitat

27 expressed in LNCaP cells and was enhanced in biochanin A-treated LNCaP cells.

28 Of the compounds tested, biochanin A was the most potent, with increased activity

29 Neoponcirin and biochanin A were identified for the first time in the Me

30 Chrysin and biochanin A were the most potent BCRP inhibitors, produc

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