Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H](C[C@@H]1O)N1C=C(F)C(=O)NC1=O.NC1=NC(C2=CC=CS2)=C2N=CN([C@H]3C[C@H](O)[C@@H](CO)O3)C2=N1

InChIKey

InChIKey=LXNIFYVUSBDTIK-BFWZIBPJSA-N

Formula

C23H26FN7O8S

Mass

579.56

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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

Not available

Substituents

Purine 2'-deoxyribonucleoside - Pyrimidine 2'-deoxyribonucleoside - Pyrimidine nucleoside - Imidazopyrimidine - Purine - Aminopyrimidine - Halopyrimidine - Pyrimidone - Aryl fluoride - Aryl halide - Hydropyrimidine - N-substituted imidazole - Primary aromatic amine - Pyrimidine - Heteroaromatic compound - Vinylogous amide - Thiophene - Oxolane - Azole - Imidazole - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Amine - Organohalogen compound - Organofluoride - Organopnictogen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organooxygen compound - Primary alcohol - Primary amine - Alcohol - Organic oxide - Hydrocarbon derivative - 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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