2072145-47-0
![2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-154658.gif "2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine Chemical Structure")
2072145-47-0
Chemical Structure
2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine
- CAS No.: 2072145-47-0
- Formula:C15H18FN3O4
- Molecular Weight:323.32
IUPAC Name: 1-((2R,3S,4R,5R)-3-fluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3-(pyridin-4-ylmethyl)-2,3-dihydropyrimidin-4(1H)-one
InChIKey: HJLCSDACYPCBHR-FAAHXZRKSA-N
SMILES: OC[C@@H]1[C@@H](O)[C@H](F)[C@H](N2CN(CC3=CC=NC=C3)C(C=C2)=O)O1
Biological Activity: 2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine is a purine nucleoside analog. 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].
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2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine | 2’-Deoxy-2’-fluoro-N3-[(pyrid-4-yl)methyl]-beta-D-arabinouridine is a purine nucleoside analog. 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. | |||||||||||||||||||||
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