40627-31-4
![7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-152578.gif "7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine Chemical Structure")
40627-31-4
Chemical Structure
7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine
- CAS No.: 40627-31-4
- Formula:C11H12N4O3
- Molecular Weight:248.24
IUPAC Name: ((1R,2R,4R,5R)-4-(4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-3,6-dioxabicyclo[3.1.0]hexan-2-yl)methanol
InChIKey: SVPYLXNTYPUWBJ-KCGFPETGSA-N
SMILES: OC[C@@H]1[C@@H](O2)[C@@H]2[C@H](N(C=C3)C4=C3C(N)=NC=N4)O1
Biological Activity: 7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine 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].
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7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine | 7-(2,3-Anhydro-β-D-ribofuranosyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine 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. | |||||||||||||||||||||
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