Structure Information
Structure

Compound Identification

SMILES

Nc1ncnc2n(cnc12)C1OC(CC([NH3+])CCC([NH3+])C([O-])=O)C(O)C1O

InChIKey

InChIKey=LMXOHSDXUQEUSF-UHFFFAOYSA-O

Formula

C15H24N7O5

Mass

382.4

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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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