Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=[14CH]N2[C@@H]1O[C@H](COC(=O)C2=CC=C(C=C2)S(F)(=O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=AQZGKOBMIMVGMG-GQTHVETBSA-N

Formula

C17H16FN5O7S

Mass

455.39

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Benzoate ester - Pentose monosaccharide - Benzoic acid or derivatives - Benzenesulfonyl group - Imidazopyrimidine - Purine - Benzoyl - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Tetrahydrofuran - Sulfonyl - Sulfonyl halide - Sulfonyl fluoride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Carboxylic acid ester - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Amine - Organic nitrogen compound - Primary amine - Organic oxygen compound - Organosulfur compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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