Structure Information
Structure

Compound Identification

SMILES

CN(C[C@H]1OC([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N)CC1=CC=C(CN)C=C1

InChIKey

InChIKey=KALQHLNRWBWZMC-XAUNWSGPSA-N

Formula

C19H25N7O3

Mass

399.455

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Purine - Imidazopyrimidine - Benzylamine - Phenylmethylamine - Aminopyrimidine - Aralkylamine - Imidolactam - Benzenoid - Monocyclic benzene moiety - Pyrimidine - Monosaccharide - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - 1,2-diol - Oxacycle - Organoheterocyclic compound - Azacycle - Primary amine - Alcohol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Primary aliphatic amine - Amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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