(±)-Equol
CAS No. 94105-90-5
(±)-Equol ( —— )
Catalog No. M19273 CAS No. 94105-90-5
Equol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora.
Purity : 98%
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 28 | In Stock |
|
10MG | 43 | In Stock |
|
25MG | 91 | In Stock |
|
50MG | 122 | In Stock |
|
100MG | 159 | In Stock |
|
200MG | 210 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product Name(±)-Equol
-
NoteResearch use only, not for human use.
-
Brief DescriptionEquol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora.
-
DescriptionEquol is a non-steroidal estrogen produced from the metabolism of the isoflavonoid phytoestrogen daidzen by human intestinal microflora.The estrogen receptor (ER) agonist activity of the naturally occurring (S)-enantiomer (EC50= 85 and 65 nM for human ERα and ERβ, respectively) is similar to that of genistein but exceeds that of daidzein.(S)-Equol preferentially binds ERβ (Ki= 0.73 nM) and demonstrates approximately 9-fold lower affinity for ERα (Ki= 6.41 nM).(S)-equol is also a potent antagonist of dihydrotestosterone, which has important implications for prostate cancer and other androgen-mediated pathologies.
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorERα; ERβ
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number94105-90-5
-
Formula Weight242.3
-
Molecular FormulaC15H14O3
-
Purity98%
-
SolubilityDMSO : ≥ 100 mg/mL; 412.76 mM
-
SMILESC1C(COc2c1ccc(c2)O)c1ccc(cc1)O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Mahalingam S, Gao L, Gonnering M, Helferich W, et al.Toxicol Appl Pharmacol. 2016 Mar 15;295:47-55.
molnova catalog
related products
-
Velnacrine
Velnacrine is a biochemical.
-
24-epi-7,8-Didehydro...
The roots of Cimicifuga foetida L.
-
R715 TFA(185052-09-9...
Potent and selective bradykinin B1 receptor antagonist (pA2 = 8.49). Displays no activity at B2 receptors. Reduces mechanical hypernociception in a mouse model of neuropathic pain. Metabolically stable.