Structure Information
Structure

Compound Identification

SMILES

Cl.CCOC(=O)C1OC(C(O)C1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=ZVHKBPIFLBGJIL-UHFFFAOYSA-N

Formula

C12H16ClN5O5

Mass

345.74

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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 - Imidazopyrimidine - Purine - Aminopyrimidine - Beta-hydroxy acid - Hydroxy acid - N-substituted imidazole - Pyrimidine - Imidolactam - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Hydrochloride - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Alcohol - Primary amine - Amine - 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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