Structure Information
Structure

Compound Identification

SMILES

COC(=O)C1=CC=CC(=C1)C(=O)CC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2OC

InChIKey

InChIKey=FRVLTOIMWHMZHH-WVSUBDOOSA-N

Formula

C21H22N4O7

Mass

442.428

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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 - Alkyl-phenylketone - Glycosyl compound - Butyrophenone - N-glycosyl compound - Benzoate ester - Hypoxanthine - Benzoic acid or derivatives - Imidazopyrimidine - Purine - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - N-substituted imidazole - Benzenoid - Monosaccharide - Pyrimidine - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Imidazole - Methyl ester - Oxolane - Ketone - Secondary alcohol - 1,2-diol - Carboxylic acid ester - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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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