Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)[C@H]1O[C@H]([C@@H](O)[C@H]1O)N1C=NC2=C1N=CN=C2N(C(=O)NC1=NC=C(Cl)C=C1)C(=O)NC1=NC=C(Cl)C=C1

InChIKey

InChIKey=LJGLCROUFKPYMM-BZDHPDOMSA-N

Formula

C24H22Cl2N10O6

Mass

617.4

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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 - Imidazopyrimidine - Purine - N-substituted imidazole - Aryl chloride - Aryl halide - Imidolactam - Pyridine - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - 1,2-diol - Carboxamide group - Urea - Secondary carboxylic acid amide - Secondary alcohol - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen 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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