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Acerca de este artículo
Fórmula empírica (notación de Hill):
C25H27NO2 · HCl · xH2O
Peso molecular:
409.95 (anhydrous basis)
UNSPSC Code:
12352203
PubChem Substance ID:
NACRES:
NA.77
MDL number:
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Permítanos ayudarleNombre del producto
(E/Z)-Endoxifen Hydrochloride Hydrate, ≥98% (HPLC)
Quality Level
assay
≥98% (HPLC)
form
solid
storage condition
desiccated
color
white to beige
solubility
DMSO: >10 mg/mL
storage temp.
2-8°C
SMILES string
O.Cl.CC\C(c1ccccc1)=C(/c2ccc(O)cc2)c3ccc(OCCNC)cc3
InChI
1S/C25H27NO2.ClH.H2O/c1-3-24(19-7-5-4-6-8-19)25(20-9-13-22(27)14-10-20)21-11-15-23(16-12-21)28-18-17-26-2;;/h4-16,26-27H,3,17-18H2,1-2H3;1H;1H2/b25-24-;;
InChI key
BISAMGUAXFFKDX-NDIQBZANSA-N
Application
(E/Z)-Endoxifen Hydrochloride Hydrate has been used:
as a selective estrogen receptor modulator (SERM) to study the role of miR-27a expression[1]
to impregnate a biocompatible polymer in the subcutaneous space adjacent to the TA muscle of PDGFRαCreER;R26NG mice
to study its in vivo performance and properties for CreERT2 (mutant estrogen receptor) control
as a selective estrogen receptor modulator (SERM) to study the role of miR-27a expression[1]
to impregnate a biocompatible polymer in the subcutaneous space adjacent to the TA muscle of PDGFRαCreER;R26NG mice
to study its in vivo performance and properties for CreERT2 (mutant estrogen receptor) control
Biochem/physiol Actions
(E/Z)-Endoxifen hydrochloride ((E/Z)-4-Hydroxy-N-desmethyltamoxifen hydrochloride) is a tamoxifen metabolite and potent Selective Estrogen Response Modifier (SERM). It is equipotent to 4-hydroxytamoxifen with respect to estrogen receptor binding and inhibition of 17-estradiol (E2)-induced cell proliferation. It is primarily catalyzed by cytochrome P450 2D6 (CYP2D6). Mutations in CYP2D6 may prevent response to tamoxifen by preventing formation of endoxifen. The gene expression patterns of five genes have been validated to be differentially regulated by endoxifen and 4-OH-Tamoxifen. Endoxifen and 4-OH-Tam have similar effects on global gene expression patterns in MCF-7 cells and the majority of the affected genes are estrogen-regulated genes.
Tamoxifen metabolite; Selective Estrogen response modifier (SERM) .
(E/Z)-endoxifen hydrochloride may be used in hormone therapy to fight breast cancer. Endoxifen is considered as an active metabolite of tamoxifen.[1] Hence it is responsible for the tamoxifen activity in the human body.
Features and Benefits
This compound is featured on the Nuclear Receptors (Steroids) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
Clase de almacenamiento
11 - Combustible Solids
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
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Contenido relacionado
We offers many products related to Nuclear Receptors (Steroids) for your research needs.
The effects of a novel hormonal breast cancer therapy, endoxifen, on the mouse skeleton
Gingery A, et al.
PLoS ONE, 9(5), e98219-e98219 (2014)
In Vivo Performance and Properties of Tamoxifen Metabolites for CreERT2 Control
Felker A, et al.
PLoS ONE, 11(4), e0152989-e0152989 (2016)
Mesenchymal Stromal Cells Are Required for Regeneration and Homeostatic Maintenance of Skeletal Muscle
Wosczyna MN, et al.
Testing, 27(7), 2029-2035 (2019)
Número de artículo de comercio global
| SKU | GTIN |
|---|---|
| E8284-5MG | 04061833608708 |
| E8284-25MG | 04061833218570 |