1612191-96-4
Chemical Structure
9-(3-Deoxy-3-fluoro-β-D-ribofuranosyl)-6-(5-phenylpyridin-3-yl)purine
- CAS. Nr.: 1612191-96-4
- Formula:C21H18FN5O3
- Molecular Weight:407.40
IUPAC Name: (2R,3S,4S,5R)-4-fluoro-5-(hydroxymethyl)-2-(6-(5-phenylpyridin-3-yl)-9H-purin-9-yl)tetrahydrofuran-3-ol
InChIKey: ULCMGCUCQXVEGD-NVEXJGOOSA-N
SMILES: F[C@H]1[C@@H](O)[C@H](N2C(N=CN=C3C4=CN=CC(C5=CC=CC=C5)=C4)=C3N=C2)O[C@@H]1CO
Biological Activity: 9-(3-Deoxy-3-fluoro-β-D-ribofuranosyl)-6-(5-phenylpyridin-3-yl)purine 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].
| Art. -Nr. | Produktname | Reinheit | Beschreibung | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
9-(3-Deoxy-3-fluoro-β-D-ribofuranosyl)-6-(5-phenylpyridin-3-yl)purine | 9-(3-Deoxy-3-fluoro-β-D-ribofuranosyl)-6-(5-phenylpyridin-3-yl)purine 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...
/
|
|||||||||||||||||||||||