Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(NC(=O)[C@]2(COC3=CC=C(CC(O)=O)C=C3)O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)C=C1

InChIKey

InChIKey=JNQGAFWHIWHZOW-XVOWXPBNSA-N

Formula

C26H26N6O7

Mass

534.529

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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 - Pentose monosaccharide - Purine - Imidazopyrimidine - Anilide - Phenoxy compound - Phenol ether - N-arylamide - Alkyl aryl ether - Aminopyrimidine - Toluene - Pyrimidine - Monosaccharide - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Imidolactam - Azole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - Secondary carboxylic acid amide - Amino acid or derivatives - 1,2-diol - Amino acid - Carboxamide group - Organoheterocyclic compound - Azacycle - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Ether - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - Primary amine - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Alcohol - 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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