1613530-43-0
Chemical Structure
5-(N-Isopentenyl-N-trifluoroacetyl) aminomethyluridine
- CAS No.: 1613530-43-0
- Formula:C17H22F3N3O7
- Molecular Weight:437.37
IUPAC Name: N-((1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)methyl)-2,2,2-trifluoro-N-(3-methylbut-2-en-1-yl)acetamide
InChIKey: IHFSIRHEIKSDFI-HKUMRIAESA-N
SMILES: O[C@H]1[C@@H](O)[C@H](N2C=C(CN(C/C=C(C)/C)C(C(F)(F)F)=O)C(NC2=O)=O)O[C@@H]1CO
Biological Activity: 5-(N-Isopentenyl-N-trifluoroacetyl) aminomethyluridine 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-(N-Isopentenyl-N-trifluoroacetyl) aminomethyluridine | 5-(N-Isopentenyl-N-trifluoroacetyl) aminomethyluridine 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...
/
|
|||||||||||||||||||||||
