Structure Information
Structure

Compound Identification

SMILES

[O-]C(=O)COC[C@H]1O[C@H]([C@H](OCC([O-])=O)[C@H]1OCC([O-])=O)N1C=NC2=C1N=C(Cl)N=C2NC1CC2CCC1C2

InChIKey

InChIKey=INCABESRMLKZEF-QNVKTGKKSA-K

Formula

C23H25ClN5O10

Mass

566.93

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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-alkylaminopurine - 6-aminopurine - Monoterpenoid - Pentose monosaccharide - Aromatic monoterpenoid - Norbornane monoterpenoid - Imidazopyrimidine - Tricarboxylic acid or derivatives - Purine - Halopyrimidine - 2-halopyrimidine - Aminopyrimidine - Aryl chloride - Imidolactam - Monosaccharide - N-substituted imidazole - Aryl halide - Pyrimidine - Heteroaromatic compound - Azole - Oxolane - Imidazole - Carboxylic acid salt - Carboxylic acid - Oxacycle - Ether - Organoheterocyclic compound - Carboxylic acid derivative - Dialkyl ether - Azacycle - Organic nitrogen compound - Amine - Organohalogen compound - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic anion - 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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