Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2[C@@H]2C[C@@H](OS(N)(=O)=O)[C@@H](O)[C@H]2O)C(N)=N1

InChIKey

InChIKey=OKPSBDFQGCZICS-ZCBVHYEASA-N

Formula

C10H15N7O5S

Mass

345.33

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted cyclopentyl nucleosides

Direct Parent

1,3-substituted cyclopentyl purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1,3-substituted cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Cyclitol or derivatives - Pyrimidine - Imidolactam - Cyclopentanol - Azole - Imidazole - Organic sulfuric acid or derivatives - Cyclic alcohol - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Azacycle - Organoheterocyclic compound - Primary amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.

External Descriptors

Not available

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