Structure Information
Structure

Compound Identification

SMILES

Cl.Cl.NC1=NC=NC2=C1N=CN2[C@@H]1O[C@@H]([C@@H](O)[C@H]1O)C(=O)N1CCN(CC(=O)NC2=CC=CC3=C2CNC3=O)CC1

InChIKey

InChIKey=VVMQSDIMNDTMII-MYXHFVDASA-N

Formula

C24H29Cl2N9O6

Mass

610.45

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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 - Alpha-amino acid amide - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Isoindolone - N-piperazineacetamide - Imidazopyrimidine - Isoindoline - Isoindole - Isoindole or derivatives - Purine - N-arylamide - Aminopyrimidine - N-alkylpiperazine - Imidolactam - N-substituted imidazole - Benzenoid - Piperazine - 1,4-diazinane - Pyrimidine - Oxolane - Heteroaromatic compound - Imidazole - Azole - Tertiary carboxylic acid amide - Amino acid or derivatives - Tertiary aliphatic amine - 1,2-diol - Lactam - Tertiary amine - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Alcohol - Carbonyl group - Hydrochloride - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organic oxide - Primary amine - Organooxygen compound - Organonitrogen 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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