Structure Information
Structure

Compound Identification

SMILES

OP(O)(O)=O.OP(O)(O)=O.OP(O)(O)=O.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)C1N=[N+]=[N-]

InChIKey

InChIKey=SHZNBVLDMGZXQM-GXYCKGFDSA-N

Formula

C10H21N8O15P3

Mass

586.24

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 2'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 2'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Pyrimidine - Imidolactam - Azole - Imidazole - Heteroaromatic compound - Oxolane - Secondary alcohol - Azo compound - Azo imide - Azacycle - Oxacycle - Organoheterocyclic compound - Primary amine - Organic nitrogen compound - Organic salt - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organonitrogen compound - Organooxygen compound - Organic zwitterion - Primary alcohol - Amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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