Structure Information
Structure

Compound Identification

SMILES

NC1=C2N=CN([C@@H]3O[C@H](CNC(=O)C[C@H]([NH3+])C([O-])=O)[C@@H](O)[C@H]3O)C2=NC=N1

InChIKey

InChIKey=LEKPSSVKGMCAIY-VWJPMABRSA-N

Formula

C14H19N7O6

Mass

381.349

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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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