Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=NC2=C1N=CN2C1OC(C(O)C1O)C(=O)NC1CC1)C#CCC1CCN(CC1)C(=O)OC1CCNC1=O

InChIKey

InChIKey=SBYSUJFXZIBZOJ-UHFFFAOYSA-N

Formula

C26H32N8O7

Mass

568.591

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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 - Purine - Imidazopyrimidine - Piperidinecarboxylic acid - Aminopyrimidine - Piperidine - Imidolactam - Pyrimidine - N-substituted imidazole - Pyrrolidone - 2-pyrrolidone - Oxolane - Pyrrolidine - Carbamic acid ester - Imidazole - Heteroaromatic compound - Azole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Lactam - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Hydrocarbon derivative - Alcohol - Carbonyl group - Organic oxide - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Primary 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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