Structure Information
Structure

Compound Identification

SMILES

N[C@H]1CC[C@@H](C[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)NC1=O

InChIKey

InChIKey=BWDKBEBWUPIWNC-RILBKXJMSA-N

Formula

C15H21N7O4

Mass

363.378

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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 - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - 3-aminopiperidine - Aminopyrimidine - Delta-lactam - Piperidinone - N-substituted imidazole - Monosaccharide - Piperidine - Imidolactam - Pyrimidine - Heteroaromatic compound - Oxolane - Imidazole - Azole - 1,2-diol - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Lactam - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Oxacycle - Organic oxygen compound - Alcohol - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Primary amine - Organooxygen compound - Amine - Primary aliphatic amine - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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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