(+/-)-Equol 雌马酚
CAS 94105-90-5 MFCD00016662
化学结构图
SMILES: OC1C=C2OCC(CC2=CC=1)C1C=CC(O)=CC=1
化学属性
| Mol. Formula | C15 |
|---|---|
| Mol. Weight | 242 |
别名和识别编码
| Chemical Name | (+/-)-Equol |
|---|---|
| MDL Number | MFCD00016662 |
| CAS Number | 94105-90-5 |
| Synonym | (±)-Equol (S)-3,4-Dihydro-3-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 3,4-Dihydro-3-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 4′,7-Dihydroxyisoflavane 3,4-Dihydro-3-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 4',7-Dihydroxyisoflavane |
| PubChem Substance ID | 135727283 |
| Beilstein Registry Number | 87752 |
| EC Number | 208-522-2 |
| Chemical Name Translation | 雌马酚 |
| Reaxys-RN | 87753 |
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分类
- {SA} Analytical Standards, Analytical/Chromatography, Bioactive Small Molecules, Cell Biology, Chemical Class, E, Phenols
- {SNA} Chemical Class, Analytical Standards, Analytical/Chromatography, Bioactive Small Molecules, Cell Biology, E, Phenols
- {SNA} Additional Standards, Analytical Standards, Chemical Class, Phenols, 分析/色谱
相关文献及参考
- [2]. Setchell KD, et al. 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. Am J Clin Nutr. 2005 May;81(5):1072-9. human intestinal bacterial flora.
- [3]. Wang J, et al. Equol promotes rat osteoblast proliferation and differentiation through activating estrogen receptor. Genet Mol Res. 2014 Jul 4;13(3):5055-63.
- [4]. Gimenez I,et al. Renal and vascular actions of equol in the rat. J Hypertens. 1997 Nov;15(11):1303-8.
- [5]. Choi EJ, et al. Anticancer mechanism of equol in 7,12-dimethylbenz(a)anthracene-treated animals. Int J Oncol. 2011 Sep;39(3):747-54.
- [6]. Charoenthongtrakul S, et al. Enhanced gastrointestinal motility with orally active ghrelin receptor agonists. J Pharmacol Exp Ther. 2009;329(3):1178-1186.
- [1]. Axelson M, et al. The identification of the weak oestrogen equol [7-hydroxy-3-(4'-hydroxyphenyl)chroman] i
