Structure Information
Structure

Compound Identification

SMILES

CN(C)C1=NC=NC2=C1N=CN2[C@H]1O[C@@H](CO)[C@@H](N)[C@H]1O

InChIKey

InChIKey=RYSMHWILUNYBFW-ZYGGXJFFSA-N

Formula

C12H18N6O3

Mass

294.315

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Dialkylarylamine - Aminopyrimidine - Monosaccharide - Imidolactam - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - 1,3-aminoalcohol - Imidazole - Oxolane - Secondary alcohol - 1,2-aminoalcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Primary aliphatic amine - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Amine - Organic nitrogen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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