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Description
- It has been used to facilitate the recombination of ect2flox allele in mouse organs.
- It has also been used to study its effect on lipopolysaccharide (LPS)-induced microglial activation.
- Protein kinase C inhibitor (IC50 = 50-200μM depending on assay conditions in MCF-7 cells or IC50 = 100μM in rat brain).
- It is a prodrug that is metabolized to active metabolites 4-hydroxytamoxifen (4-OHT) and endoxifen by cytochrome P450 isoforms CYP2D6 and CYP3A4.
Specifications
Specifications
| Melting Point | 96°C to 100°C |
| Color | White |
| Loss on Drying | 0.0021 |
| Refractive Index | KR5919600 |
| Quantity | 5 g |
| Synonym | [Z]-1-[p-Dimethylaminoethoxyphenyl]-1,2-diphenyl-1-butene, (Z)-2-[4-(1,2-Diphenyl-1-butenyl)phenoxy]-N,N-dimethylethanamine, ICI 47699, trans-Tamoxifen |
| Solubility Information | Practically insoluble in water (< 0.01% at 20°C); soluble in methanol, ethanol, 2-propanol, propyleneglycol, chloroform (50mg/mL - clear, colorless to faint yellow solution) or DMSO |
| IUPAC Name | (2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethyl)dimethylamine |
| Physical Form | Powder |
| Assay | 0.9935 |
Safety and Handling
| storageNote1 | Store at +4°C. |
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