Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C25H27NO.ClH |
| Molecular Weight | 393.949 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC\C(=C(/C1=CC=CC=C1)C2=CC=C(OCCNC)C=C2)C3=CC=CC=C3
InChI
InChIKey=GMLHJWZEYLTNJW-BJFQDICYSA-N
InChI=1S/C25H27NO.ClH/c1-3-24(20-10-6-4-7-11-20)25(21-12-8-5-9-13-21)22-14-16-23(17-15-22)27-19-18-26-2;/h4-17,26H,3,18-19H2,1-2H3;1H/b25-24-;
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C25H27NO |
| Molecular Weight | 357.488 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| The tamoxifen metabolite, endoxifen, is a potent antiestrogen that targets estrogen receptor alpha for degradation in breast cancer cells. | 2009-03-01 |
|
| Association of tamoxifen (TAM) and TAM metabolite concentrations with self-reported side effects of TAM in women with breast cancer. | 2004-05 |
|
| Active tamoxifen metabolite plasma concentrations after coadministration of tamoxifen and the selective serotonin reuptake inhibitor paroxetine. | 2003-12-03 |
|
| Reversible and irreversible inhibition of CYP3A enzymes by tamoxifen and metabolites. | 2002-10 |
|
| Peroxidase activation of tamoxifen and toremifene resulting in DNA damage and covalently bound protein adducts. | 1995-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 17:30:22 GMT 2025
by
admin
on
Wed Apr 02 17:30:22 GMT 2025
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| Record UNII |
6AP7YK59KS
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| Record Status |
Validated (UNII)
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| Record Version |
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6AP7YK59KS
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15917-65-4
Created by
admin on Wed Apr 02 17:30:22 GMT 2025 , Edited by admin on Wed Apr 02 17:30:22 GMT 2025
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