Structure Information
Structure

Compound Identification

SMILES

COC1C(OC(C)=O)C(COC(C)=O)OC1N1C=NC2=C1N=C(NC(C)=O)N=C2Cl

InChIKey

InChIKey=JFZCRBCMCNIGII-UHFFFAOYSA-N

Formula

C17H20ClN5O7

Mass

441.83

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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 - N-glycosyl compound - Glycosyl compound - N-acetylarylamine - Imidazopyrimidine - Purine - N-arylamide - Halopyrimidine - Aryl halide - Aryl chloride - Pyrimidine - Dicarboxylic acid or derivatives - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Acetamide - Azole - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid ester - Carboxylic acid derivative - Dialkyl ether - Oxacycle - Ether - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - 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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