Structure Information
Structure

Compound Identification

SMILES

NC(CC[C@H](N)C(O)=O)C[C@H]1OC([C@H](O)[C@@H]1O)N1C=CC(=O)NC1=O

InChIKey

InChIKey=BPZYAHBYZPURAF-WRDBXGHFSA-N

Formula

C14H22N4O7

Mass

358.351

Export to:

JSON SDF CSV

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 heteromonocyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Alpha-amino acid - Alpha-amino acid or derivatives - L-alpha-amino acid - Pentose monosaccharide - Medium-chain fatty acid - Amino fatty acid - Heterocyclic fatty acid - Hydroxy fatty acid - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Fatty acyl - Fatty acid - Vinylogous amide - Oxolane - Heteroaromatic compound - Urea - Secondary alcohol - Amino acid or derivatives - Lactam - 1,2-diol - Amino acid - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Primary aliphatic amine - Alcohol - Carbonyl group - Organic oxide - Organonitrogen compound - Organooxygen compound - Primary amine - Amine - Organic nitrogen compound - Aromatic heteromonocyclic 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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

Previous Back Next