For research use only. Not for therapeutic Use.
Tamoxifen-d5 is a deuterated form of tamoxifen, where five hydrogen atoms have been replaced with deuterium. This isotopically labeled compound is primarily used in pharmaceutical research to study the metabolism, pharmacokinetics, and pharmacodynamics of tamoxifen, a widely used selective estrogen receptor modulator (SERM) for the treatment and prevention of breast cancer. The deuterium labeling allows for precise tracking in analytical methods such as mass spectrometry, providing enhanced stability and accuracy in monitoring the drug’s distribution and metabolic pathways within the body. Tamoxifen-d5 is an invaluable tool for researchers aiming to optimize breast cancer therapies, assess drug interactions, and better understand the mechanisms of action and resistance associated with tamoxifen.
Catalog Number | R003188 |
CAS Number | 157698-32-3 |
Synonyms | (Z)-1-[4-[2-(Dimethylamino)ethoxy]phenyl]-1,2-diphenyl-1-butene-3,3,4,4,4-d5; ?(Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine-d5; ICI 47699-d5; Mammaton-d5; Novaldex-d5; Tamoxifen-d5; Z-Tamoxifen-d5; trans-Tamoxifen-d5; |
Molecular Formula | C26H24D5NO |
Purity | ≥95% |
Target | Metabolic Enzyme/Protease |
Storage | 4°C |
IUPAC Name | N,N-dimethyl-2-[4-[(Z)-3,3,4,4,4-pentadeuterio-1,2-diphenylbut-1-enyl]phenoxy]ethanamine |
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-/i1D3,4D2 |
InChIKey | NKANXQFJJICGDU-FUYVPVGLSA-N |
SMILES | [2H]C([2H])([2H])C([2H])([2H])/C(=C(\C1=CC=CC=C1)/C2=CC=C(C=C2)OCCN(C)C)/C3=CC=CC=C3 |