Structure Information
Structure

Compound Identification

SMILES

CSC(=S)NC1C(CO)OC(C1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=ZLCNIBLSJRHZBL-UHFFFAOYSA-N

Formula

C12H16N6O3S2

Mass

356.42

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Primary aromatic amine - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Dithiocarbamic acid ester - Secondary alcohol - Sulfenyl compound - Organoheterocyclic compound - Oxacycle - Azacycle - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Primary alcohol - Primary amine - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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