Structure Information
Structure

Compound Identification

SMILES

CCCSS[C@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C=NC2=C1N=C(N)N=C2Cl

InChIKey

InChIKey=BAZJISCAVWVQDB-QRKAXHLRSA-N

Formula

C13H18ClN5O3S2

Mass

391.89

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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 - Imidazopyrimidine - Purine - Aminopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - Dialkyldisulfide - Secondary alcohol - Organic disulfide - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Organohalogen compound - Primary alcohol - Primary amine - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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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