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(+/-)-EQUOL

(+/-)-EQUOL Structure
CAS No.
94105-90-5
Chemical Name:
(+/-)-EQUOL
Synonyms
NV 07α;(+/-)Equol;(+/-)-EQUOL;Equol,99%e.e.;EQUOL(RACEMIC);(+/-)-Equol>(+/-)-Equol (GMP);4',7-Isoflavandiol;7,4'-HoMoisoflavane;(±)-EQUOL >= 99.0% (TLC)
CBNumber:
CB8972097
Molecular Formula:
C15H14O3
Molecular Weight:
242.27
MOL File:
94105-90-5.mol
MSDS File:
SDS
Modify Date:
2024/8/22 14:21:17

(+/-)-EQUOL Properties

Melting point 158-160?C
Boiling point 441.7±45.0 °C(Predicted)
Density 1.286±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility soluble in Ethanol
form Crystalline powder
pka 9.94±0.40(Predicted)
color White to Light yellow to Light red
Water Solubility Soluble in DMSO and methanol or 100% ethanol. Insoluble in water.
Sensitive Hygroscopic
BRN 87752
InChI InChI=1S/C15H14O3/c16-13-4-1-10(2-5-13)12-7-11-3-6-14(17)8-15(11)18-9-12/h1-6,8,12,16-17H,7,9H2
InChIKey ADFCQWZHKCXPAJ-UHFFFAOYSA-N
SMILES C1OC2=CC(O)=CC=C2CC1C1=CC=C(O)C=C1

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H332-H335
Precautionary statements  P261-P280-P305+P351+P338
WGK Germany  3
HS Code  2932990090

(+/-)-EQUOL price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 45405 (±)-Equol ≥99.0% (TLC) 94105-90-5 1MG ₹26781.05 2022-06-14 Buy
Sigma-Aldrich(India) 45405 (±)-Equol ≥99.0% (TLC) 94105-90-5 5MG ₹88678.4 2022-06-14 Buy
TCI Chemicals (India) E0922 (±)-Equol min. 98.0 % 94105-90-5 200MG ₹8800 2022-05-26 Buy
Product number Packaging Price Buy
45405 1MG ₹26781.05 Buy
45405 5MG ₹88678.4 Buy
E0922 200MG ₹8800 Buy

(+/-)-EQUOL Chemical Properties,Uses,Production

Description

Equol is a nonsteroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzein by human intestinal microflora. The estrogen receptor (ER) binding activity of the naturally occurring (S)-enantiomer demonstrates greater affinity toward ERβ while the (R)-enantiomer demonstrates greater affinity towards ERα. Synthesized as a racemic mixture, (±)-equol exhibits EC50 values of 200 and 74 nM for human ERα and ERβ, respectively and induces breast cancer cell proliferation in vitro at concentrations as low as 100 nM.

Chemical Properties

White to Off-White Solid

Uses

(+/-)-Equol exhibits EC50 values of 200 and 74 nM for human ERα and ERβ, respectively and induces breast cancer cell proliferation in vitro at concentrations as low as 100 nM. It is a weak estrogenic agonist, and competitive inhibitor of 17β-estradiol at the estradiol receptor. It inhibits 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced neoplastic cell transformation by targeting the MEK/ERK/p90RSK/activator protein-1 signalling pathway. It functions as a DHT blocker.

Application

(±)-Equol is a metabolite produced in vivo from the soy phytoestrogen daidzein by the action of certain gut microflora, and is a nonsteroidal estrogen of the isoflavonoid class. (±)-Equo has been reported to have estrogenic activity and affinity for estrogen receptors. (±)-Equo can exist in two enantiomeric forms, (S)-equol and (R)-equol. In binding assays, (S)-equol has a higher binding affinity for estrogen β receptors.

Biological Activity

Metabolite of daidzein. Weak estrogenic agonist, and competitive inhibitor of 17β-estradiol at the estradiol receptor.
(R,S)-Equol is a flavonoid. Racemic mixture. This is a metabolite that is produced in vivo from soy phytoestrogen daidzein from gut microflora. (R,S)-Equol inhibits 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced neoplastic cell transformation by targeting the MEK/ERK/p90RSK/activator protein-1 signalling pathway. (R,S)-Equol shows positive effects on the incidence of prostate cancer. Functions as a DHT blocker. Preferentially activates estrogen receptor β (ERβ).

References

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
R. S. Muthyala, Y. H. Ju, S. Sheng, L. D. Williams, D. R. Doerge, B. S. Katzenellenbogen, W. G. Helferich, J. A. Katzenellenbogen, Bioorg. Med. Chem. 2004, 12, 1559.
Isolation and identification of new bacterial stains producing equol from Pueraria lobate extract fermentation
J. E. Kwon, J. Lim, I. Kim, D. Kim, S. C. Kang, PLoS ONE 2018, 13, e0192490.
Setchell, K.D.R., Clerici, C., Lephart, E.D., et al. S-equol, a potent ligand for estrogen receptor β, is the exclusive enantiomeric form of the soy isoflavone metabolite produced by human intestinal bacterial flora. Am. J. Clin. Nutr. 81(5), 1072-1079 (2005).
Liu, H., Du, J., Hu, C., et al. Delayed activation of extracellular-signal-regulated kinase ? is involved in genistein- and equol-induced cell proliferation and estrogen-receptor-α-mediated transcription in MCF-7 breast cancer cells. Journal of Nutritional Biochemistry (2009).

(+/-)-EQUOL Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 140)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Gagri Global IT Services Pvt. Ltd. +91-40-27170174, Telangana, India 1321 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
Hangzhou Weitai Biological Pharmaceutical Co.,Ltd. +8613282012786 China 61 58 Inquiry
Wuhan Nutra Biotechnology Co.,Ltd +8617786394783 China 300 58 Inquiry
Qingdao Yonghefeng Economic and Trade Co., Ltd. +86-13375559818 +86-13375559818 China 195 58 Inquiry
Hebei Chuanghai Biotechnology Co,.LTD +86-13131129325 China 5895 58 Inquiry
Chongqing Zhihe Biopharmaceutical Co., Ltd. +8618580541567 China 303 58 Inquiry

94105-90-5((+/-)-EQUOL)Related Search:

7,4'-HoMoisoflavane NV 07α 3-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol 7-Hydroxy-3-(4-hydroxyphenyl)chroman 4',7-Isoflavandiol 3,4-Dihydro-3-(4-hydroxyphenyl)-2H-chromen-7-ol, (+/-)-Equol, 4',7-Isoflavandiol, 7-Hydroxy-3-(4-hydroxyphenyl)chroman 4',7-Isoflavandiol, (+/-)-Equol 4′,7-Dihydroxyisoflavane (+/-)-Equol (GMP) (±)-EQUOL >= 99.0% (TLC) Equol,99%e.e. 3,4-dihydro-3-(4-hydroxyphenyl)-2h-1-benzopyran-7-ol EQUOL(RACEMIC) (+/-)-7-Hydroxy-3-(4-hydroxyphenyl)chroman (+/-)-3,4-Dihydro-3-(4-hydroxyphenyl)-2H-chromen-7-ol, (+/-)-Equol Anti hair loss s equol 94105-90-5 s-equol powder 99% purity equol Equol,3-(4-Hydroxyphenyl)-7-chromanol Nano Liposomal Equol,3-(4-Hydroxyphenyl)-7-chromanol (+/-)-Equol> 2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(4-hydroxyphenyl)- (+/-)Equol (+/-)-EQUOL ((2R,3S)-3-acetoxy-5-methoxytetrahydrofuran-2-yl)methyl acetate 3-(4-Hydroxyphenyl)-7-chromanol inhibit,Estrogen Receptor/ERR,Drug Metabolite,(±) Equol,(±)Equol,(±)-Equol,Inhibitor (±)-Equol/2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(4-hydroxyphenyl)- 4',7-Isoflavandiol 94105-90-5 Metabolites metabolite Aromatics Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals