Structure Information
Structure

Compound Identification

SMILES

[H][C@](N)(CC[C@]([H])(N)C(O)=O)C[C@@]1([H])O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=LMXOHSDXUQEUSF-YECHIGJVSA-N

Formula

C15H23N7O5

Mass

381.393

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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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

CHEBI:45453 : adenosines - non-proteinogenic alpha-amino acid

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