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Items: 1 to 20 of 96

1.

Equol: history, chemistry, and formation.

Setchell KD, Clerici C.

J Nutr. 2010 Jul;140(7):1355S-62S. doi: 10.3945/jn.109.119776. Epub 2010 Jun 2. Review.

2.

S-equol, a potent ligand for estrogen receptor beta, is the exclusive enantiomeric form of the soy isoflavone metabolite produced by human intestinal bacterial flora.

Setchell KD, Clerici C, Lephart ED, Cole SJ, Heenan C, Castellani D, Wolfe BE, Nechemias-Zimmer L, Brown NM, Lund TD, Handa RJ, Heubi JE.

Am J Clin Nutr. 2005 May;81(5):1072-9.

PMID:
15883431
3.

Equol: pharmacokinetics and biological actions.

Setchell KD, Clerici C.

J Nutr. 2010 Jul;140(7):1363S-8S. doi: 10.3945/jn.109.119784. Epub 2010 Jun 2. Review.

4.

The pharmacokinetic behavior of the soy isoflavone metabolite S-(-)equol and its diastereoisomer R-(+)equol in healthy adults determined by using stable-isotope-labeled tracers.

Setchell KD, Zhao X, Jha P, Heubi JE, Brown NM.

Am J Clin Nutr. 2009 Oct;90(4):1029-37. doi: 10.3945/ajcn.2009.27981. Epub 2009 Aug 26.

5.

Metabolism of dietary soy isoflavones to equol by human intestinal microflora--implications for health.

Yuan JP, Wang JH, Liu X.

Mol Nutr Food Res. 2007 Jul;51(7):765-81. Review.

PMID:
17579894
6.

The clinical importance of the metabolite equol-a clue to the effectiveness of soy and its isoflavones.

Setchell KD, Brown NM, Lydeking-Olsen E.

J Nutr. 2002 Dec;132(12):3577-84. Review.

PMID:
12468591
7.

The role of colonic bacteria in the metabolism of the natural isoflavone daidzin to equol.

Rafii F.

Metabolites. 2015 Jan 14;5(1):56-73. doi: 10.3390/metabo5010056. Review.

8.
9.

S-(-)equol producing status not associated with breast cancer risk among low isoflavone-consuming US postmenopausal women undergoing a physician-recommended breast biopsy.

Virk-Baker MK, Barnes S, Krontiras H, Nagy TR.

Nutr Res. 2014 Feb;34(2):116-25. doi: 10.1016/j.nutres.2013.12.002. Epub 2013 Dec 18.

10.
11.

The pharmacokinetics of S-(-)equol administered as SE5-OH tablets to healthy postmenopausal women.

Setchell KD, Zhao X, Shoaf SE, Ragland K.

J Nutr. 2009 Nov;139(11):2037-43. doi: 10.3945/jn.109.110874. Epub 2009 Sep 23.

PMID:
19776178
12.

Daidzein and genistein are converted to equol and 5-hydroxy-equol by human intestinal Slackia isoflavoniconvertens in gnotobiotic rats.

Matthies A, Loh G, Blaut M, Braune A.

J Nutr. 2012 Jan;142(1):40-6. doi: 10.3945/jn.111.148247. Epub 2011 Nov 23.

PMID:
22113864
13.

Metabolomics reveals differences between three daidzein metabolizing phenotypes in adults with cardiometabolic risk factors.

Reverri EJ, Slupsky CM, Mishchuk DO, Steinberg FM.

Mol Nutr Food Res. 2017 Jan;61(1). doi: 10.1002/mnfr.201600132. Epub 2016 Aug 3.

PMID:
27364093
14.

Production of phytoestrogen S-equol from daidzein in mixed culture of two anaerobic bacteria.

Wang XL, Kim HJ, Kang SI, Kim SI, Hur HG.

Arch Microbiol. 2007 Feb;187(2):155-60. Epub 2006 Nov 16.

PMID:
17109177
15.

The chemopreventive action of equol enantiomers in a chemically induced animal model of breast cancer.

Brown NM, Belles CA, Lindley SL, Zimmer-Nechemias LD, Zhao X, Witte DP, Kim MO, Setchell KD.

Carcinogenesis. 2010 May;31(5):886-93. doi: 10.1093/carcin/bgq025. Epub 2010 Jan 28.

17.

Equol, a natural estrogenic metabolite from soy isoflavones: convenient preparation and resolution of R- and S-equols and their differing binding and biological activity through estrogen receptors alpha and beta.

Muthyala RS, Ju YH, Sheng S, Williams LD, Doerge DR, Katzenellenbogen BS, Helferich WG, Katzenellenbogen JA.

Bioorg Med Chem. 2004 Mar 15;12(6):1559-67.

PMID:
15018930
18.

Is equol the key to the efficacy of soy foods?

Lampe JW.

Am J Clin Nutr. 2009 May;89(5):1664S-1667S. doi: 10.3945/ajcn.2009.26736T. Epub 2009 Apr 8.

19.

Enantioselective synthesis of S-equol from dihydrodaidzein by a newly isolated anaerobic human intestinal bacterium.

Wang XL, Hur HG, Lee JH, Kim KT, Kim SI.

Appl Environ Microbiol. 2005 Jan;71(1):214-9.

20.

Serum steroid hormones, sex hormone-binding globulin concentrations, and urinary hydroxylated estrogen metabolites in post-menopausal women in relation to daidzein-metabolizing phenotypes.

Frankenfeld CL, McTiernan A, Tworoger SS, Atkinson C, Thomas WK, Stanczyk FZ, Marcovina SM, Weigle DS, Weiss NS, Holt VL, Schwartz SM, Lampe JW.

J Steroid Biochem Mol Biol. 2004 Apr;88(4-5):399-408.

PMID:
15145450

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