89128-99-4
![5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-152735.gif "5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine Chemical Structure")
Chemical Structure
5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine
- CAS No.: 89128-99-4
- Formula:C13H16F3N3O6S
- Molecular Weight:399.34
IUPAC Name: N-((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl)-2,2,2-trifluoro-N-methylacetamide
InChIKey: JSJWOXIZNRMGDB-FDDDBJFASA-N
SMILES: O[C@H]1[C@@H](O)[C@H](N2C=C(CN(C)C(C(F)(F)F)=O)C(NC2=S)=O)O[C@@H]1CO
Biological Activity: 5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine | 5-[[Methyl(2,2,2-trifluoroacetyl)amino]methyl]-2-thiouridine is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
