Structure Information
Structure

Compound Identification

SMILES

CN(C)C1=NC=NC2=C1N=CN2[C@H]1O[C@@H](CO)[C@@H]([NH3+])[C@@H]1O

InChIKey

InChIKey=RYSMHWILUNYBFW-LUCMMUEDSA-O

Formula

C12H19N6O3

Mass

295.322

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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 - Imidolactam - Monosaccharide - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - 1,3-aminoalcohol - Quaternary ammonium salt - Secondary alcohol - 1,2-aminoalcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organooxygen compound - Hydrocarbon derivative - Primary aliphatic amine - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Alcohol - Amine - Primary alcohol - Primary amine - Organic cation - 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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