Structure Information
Structure

Compound Identification

SMILES

CC1=CN([C@H]2C[C@H](OP([O-])(=S)OC[C@H]3O[C@H](C[C@@H]3O)N3C=NC4=C3N=CN=C4N)[C@@H](COP([O-])(=S)O[C@H]3C[C@@H](O[C@@H]3CO)N3C=CC(=O)NC3=O)O2)C(=O)NC1=O

InChIKey

InChIKey=ZQCBOQOHEJAGKU-DYTVHUQLSA-L

Formula

C29H35N9O15P2S2

Mass

875.72

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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 - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Thiophosphoric acid ester - Primary aromatic amine - Pyrimidine - Imidolactam - Organic thiophosphoric acid or derivatives - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary alcohol - Lactam - Azacycle - Oxacycle - Organoheterocyclic compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Primary amine - Organic oxide - Alcohol - Organopnictogen compound - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Primary alcohol - Organic anion - 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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