Structure Information
Structure

Compound Identification

SMILES

CS(=O)(=O)OC[C@@H]1[C@H](COCC2=CC=CC=C2)[C@H](OCC2=CC=CC=C2)[C@H]1N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=NTUPBDROZWMILN-KJBBBAAKSA-N

Formula

C26H29N5O5S

Mass

523.61

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclobutyl nucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Cyclobutyl nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Cyclobutyl purine nucleoside - Cyclobutyl nucleoside - 6-aminopurine - Benzylether - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid ester - Sulfonic acid ester - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Imidazole - Methanesulfonate - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Amine - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as cyclobutyl 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 or pyrimidine base.

External Descriptors

Not available

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