(E/Z)-4-hydroxy Tamoxifen

Modify Date: 2024-01-02 16:03:05

(E/Z)-4-hydroxy Tamoxifen Structure
(E/Z)-4-hydroxy Tamoxifen structure
Common Name (E/Z)-4-hydroxy Tamoxifen
CAS Number 68392-35-8 Molecular Weight 387.51400
Density 1.092 Boiling Point N/A
Molecular Formula C26H29NO2 Melting Point 135-144°C
MSDS Chinese USA Flash Point N/A
Symbol GHS07 GHS08
GHS07, GHS08
Signal Word Warning

 Use of (E/Z)-4-hydroxy Tamoxifen


(E/Z)-4-Hydroxytamoxifen is a racemic compound of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen isomers. (E/Z)-4-Hydroxytamoxifen is an estrogen receptor modulator.

 Names

Name Afimoxifene
Synonym More Synonyms

 (E/Z)-4-hydroxy Tamoxifen Biological Activity

Description (E/Z)-4-Hydroxytamoxifen is a racemic compound of (Z)-4-Hydroxytamoxifen and (E)-4-Hydroxytamoxifen isomers. (E/Z)-4-Hydroxytamoxifen is an estrogen receptor modulator.
Related Catalog
Target

Estrogen receptor

 Chemical & Physical Properties

Density 1.092
Melting Point 135-144°C
Molecular Formula C26H29NO2
Molecular Weight 387.51400
Exact Mass 387.22000
PSA 32.70000
LogP 5.70170
Appearance of Characters white to off-white
Storage condition Refrigerator
Water Solubility methanol: soluble10mg/mL

 Safety Information

Symbol GHS07 GHS08
GHS07, GHS08
Signal Word Warning
Hazard Statements H302-H312-H332-H361
Precautionary Statements P280
Personal Protective Equipment Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges
Hazard Codes Xn
Risk Phrases 63-20/21/22
Safety Phrases 22-23-36
RIDADR NONH for all modes of transport
RTECS SL1210000

 Articles179

More Articles
Combined histone deacetylase inhibition and tamoxifen induces apoptosis in tamoxifen-resistant breast cancer models, by reversing Bcl-2 overexpression.

Breast Cancer Res. 17 , 26, (2015)

The emergence of hormone therapy resistance, despite continued expression of the estrogen receptor (ER), is a major challenge to curing breast cancer. Recent clinical studies suggest that epigenetic m...

Selective inhibition of RET mediated cell proliferation in vitro by the kinase inhibitor SPP86.

BMC Cancer 14 , 853, (2014)

The RET tyrosine kinase receptor has emerged as a target in thyroid and endocrine resistant breast cancer. We previously reported the synthesis of kinase inhibitors with potent activity against RET. H...

Pharmacological inhibition of dynamin II reduces constitutive protein secretion from primary human macrophages.

PLoS ONE 9(10) , e111186, (2014)

Dynamins are fission proteins that mediate endocytic and exocytic membrane events and are pharmacological therapeutic targets. These studies investigate whether dynamin II regulates constitutive prote...

 Synonyms

Propiophenone,4'-[2-(diethylamino)ethoxy]-,hydrochloride
1-[4-(2-Diaethylamino-aethoxy)-phenyl]-propan-1-on,Hydrochlorid
1-[4-(2-diethylaminoethyloxy)phenyl]propan-1-one hydrochloride
4-hydroxytamoxifene
1-[4-(2-dimethylaminoethoxy)phenyl]-1-(4-hydroxyphenyl)-2-phenylbut-1-ene
(E,Z)-4-hydroxytamoxifen
1-[4-(2-diethylamino-ethoxy)-phenyl]-propan-1-one,hydrochloride
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