Structure Information
Structure

Compound Identification

SMILES

[O-]C(=O)C(F)(F)F.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COS(=O)(=O)NC(=O)CC[NH3+])[C@@H](O)[C@H]1O

InChIKey

InChIKey=JRSVSOWUYZPCGS-CRDPPMACSA-N

Formula

C15H20F3N7O9S

Mass

531.42

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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

Not available

Substituents

Purine nucleoside - Beta amino acid or derivatives - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Imidolactam - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Organic sulfuric acid or derivatives - Alpha-halocarboxylic acid or derivatives - Alpha-halocarboxylic acid - Oxolane - Quaternary ammonium salt - Amino acid or derivatives - Carboxylic acid salt - 1,2-diol - Secondary alcohol - Oxacycle - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic zwitterion - Hydrocarbon derivative - Primary aliphatic amine - Organic nitrogen compound - Carbonyl group - Organic oxide - Organohalogen compound - Organic oxygen compound - Organofluoride - Amine - Organonitrogen compound - Organooxygen compound - Alkyl halide - Alkyl fluoride - Primary amine - Alcohol - 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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