(E)-Tamoxifen

CAS: 13002-65-8

Ref. 3D-FT27995

Product Information

• Name: (E)-Tamoxifen
• Synonyms: 2-[4-[(1E)-1,2-Diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl-ethanamine2-[p-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethyl-ethylamine cis-Tamoxifen, 2-[4-[(1E)-1,2-Diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethylethanamine, Brn 2062021, Ethanamine, 2-(4-(1,2-diphenyl-1-butenyl)phenoxy)-N,N-dimethyl-, (E)-, Ethanamine, 2-[4-[(1E)-1,2-diphenyl-1-buten-1-yl]phenoxy]-N,N-dimethyl-, Ethanamine, 2-[4-[(1E)-1,2-diphenyl-1-butenyl]phenoxy]-N,N-dimethyl-, Ethylamine, 2-[p-(1,2-diphenyl-1-butenyl)phenoxy]-N,N-dimethyl-, (E)-, Ethylamine, N,N-dimethyl-2-(p-(1,2-diphenyl-1-butenyl)phenoxy)-, (E)-, Tamoxifen (E), cis-Tamoxifen
• CAS: 13002-65-8

Description

Tamoxifen is a drug that belongs to the group of antiestrogens. It is used in cancer treatment and is administered orally, intravenously, or by intramuscular injection. Tamoxifen has been shown to bind to estrogen receptors and inhibit the growth of estrogen-dependent breast cancer cells. Tamoxifen also has a number of metabolites, which are formed through reactions with reactive functional groups such as hydroxyl and cyano groups. These metabolites can be detected using magnetic resonance spectroscopy (MRS) and nuclear magnetic resonance (NMR). Some of these metabolites have been shown to have an effect on cell nuclei, including binding to DNA or altering the activity of enzymes involved in DNA synthesis.

• Brand: Biosynth

Chemical properties

• Molecular weight: 371.52 g/mol
• Formula: C₂₆H₂₉NO
• Purity: Min. 98 Area-%
• Color/Form: Powder
• InChI: InChI=1S/C26H29NO/c1-4-25(21-11-7-5-8-12-21)26(22-13-9-6-10-14-22)23-15-17-24(18-16-23)28-20-19-27(2)3/h5-18H,4,19-20H2,1-3H3/b26-25+
• InChI key: InChIKey=NKANXQFJJICGDU-OCEACIFDSA-N
• SMILES: CC/C(=C(/c1ccccc1)c1ccc(OCCN(C)C)cc1)c1ccccc1