1611486-54-4
![4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-152827.gif "4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine Chemical Structure")
1611486-54-4
Chemical Structure
4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine
- CAS No.: 1611486-54-4
- Formula:C11H15N5O5
- Molecular Weight:297.27
IUPAC Name: (2R,3R,4S,5R)-2-(6-amino-4-methoxy-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
InChIKey: OTGAOSCWXAHXOA-DAGMQNCNSA-N
SMILES: OC[C@@H]1[C@@H](O)[C@@H](O)[C@H](N(N=C2)C3=C2C(OC)=NC(N)=N3)O1
Biological Activity: 4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine 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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4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine | 4-Methoxy-1-β-D-ribofuranosyl-1H-pyrazolo[3,4-d]pyrimidin-6-amine 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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