에쿠올 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "에쿠올" in Korean language version.

refsWebsite

Global rank Korean rank

4^th place

2^nd place

3^rd place

6,663^rd place

2,136^th place

1^st place

5^th place

11^th place

1,389^th place

550^th place

aspetjournals.org

The structures of 7,4’-dihydroxy-isoflavan and its precursors is shown in Structural Elucidation of Hydroxylated Metabolites of the Isoflavan Equol by GC/MS and HPLC/MS Archived 2008년 9월 5일 - 웨이백 머신 by Corinna E. Rüfer, Hansruedi Glatt, and Sabine E. Kulling in Drug Metabolism and Disposition (2005, electronic publication).

Wang XL, Hur HG, Lee JH, Kim KT, Kim SI (January 2005). “Enantioselective synthesis of S-equol from dihydrodaidzein by a newly isolated anaerobic human intestinal bacterium”. 《Appl. Environ. Microbiol.》 71 (1): 214–9. doi:10.1128/AEM.71.1.214-219.2005. PMC 544246. PMID 15640190.
Muthyala, Rajeev S; Ju, Young H; Sheng, Shubin; Williams, Lee D; Doerge, Daniel R; Katzenellenbogen, Benita S; Helferich, William G; Katzenellenbogen, John A (2004). “Equol, a natural estrogenic metabolite from soy isoflavones”. 《Bioorganic & Medicinal Chemistry》 12 (6): 1559–1567. doi:10.1016/j.bmc.2003.11.035. ISSN 0968-0896. PMID 15018930.
Frankenfeld CL, Atkinson C, Thomas WK, 외. (December 2005). “High concordance of daidzein-metabolizing phenotypes in individuals measured 1 to 3 years apart”. 《Br. J. Nutr.》 94 (6): 873–6. doi:10.1079/bjn20051565. PMID 16351761.
Setchell, Kenneth D. R.; Carlo Clerici (2010년 6월 2일). “Equol: history, chemistry, and formation”. 《J Nutr》 140 (7): 1355S–62S. doi:10.3945/jn.109.119776. PMC 2884333. PMID 20519412.
Mueller SO, Simon S, Chae K, Metzler M, Korach KS (April 2004). “Phytoestrogens and their human metabolites show distinct agonistic and antagonistic properties on estrogen receptor {α} (ER{α}) and ERβ in human cells”. 《Toxicol. Sci.》 80 (1): 14–25. doi:10.1093/toxsci/kfh147. PMID 15084758.

Wang XL, Hur HG, Lee JH, Kim KT, Kim SI (January 2005). “Enantioselective synthesis of S-equol from dihydrodaidzein by a newly isolated anaerobic human intestinal bacterium”. 《Appl. Environ. Microbiol.》 71 (1): 214–9. doi:10.1128/AEM.71.1.214-219.2005. PMC 544246. PMID 15640190.
Muthyala, Rajeev S; Ju, Young H; Sheng, Shubin; Williams, Lee D; Doerge, Daniel R; Katzenellenbogen, Benita S; Helferich, William G; Katzenellenbogen, John A (2004). “Equol, a natural estrogenic metabolite from soy isoflavones”. 《Bioorganic & Medicinal Chemistry》 12 (6): 1559–1567. doi:10.1016/j.bmc.2003.11.035. ISSN 0968-0896. PMID 15018930.
Frankenfeld CL, Atkinson C, Thomas WK, 외. (December 2005). “High concordance of daidzein-metabolizing phenotypes in individuals measured 1 to 3 years apart”. 《Br. J. Nutr.》 94 (6): 873–6. doi:10.1079/bjn20051565. PMID 16351761.
Setchell, Kenneth D. R.; Carlo Clerici (2010년 6월 2일). “Equol: history, chemistry, and formation”. 《J Nutr》 140 (7): 1355S–62S. doi:10.3945/jn.109.119776. PMC 2884333. PMID 20519412.
Mueller SO, Simon S, Chae K, Metzler M, Korach KS (April 2004). “Phytoestrogens and their human metabolites show distinct agonistic and antagonistic properties on estrogen receptor {α} (ER{α}) and ERβ in human cells”. 《Toxicol. Sci.》 80 (1): 14–25. doi:10.1093/toxsci/kfh147. PMID 15084758.

The structures of 7,4’-dihydroxy-isoflavan and its precursors is shown in Structural Elucidation of Hydroxylated Metabolites of the Isoflavan Equol by GC/MS and HPLC/MS Archived 2008년 9월 5일 - 웨이백 머신 by Corinna E. Rüfer, Hansruedi Glatt, and Sabine E. Kulling in Drug Metabolism and Disposition (2005, electronic publication).

Muthyala, Rajeev S; Ju, Young H; Sheng, Shubin; Williams, Lee D; Doerge, Daniel R; Katzenellenbogen, Benita S; Helferich, William G; Katzenellenbogen, John A (2004). “Equol, a natural estrogenic metabolite from soy isoflavones”. 《Bioorganic & Medicinal Chemistry》 12 (6): 1559–1567. doi:10.1016/j.bmc.2003.11.035. ISSN 0968-0896. PMID 15018930.