Structure Information
Structure

Compound Identification

SMILES

CC(NC(=O)OCC1=CC=CC=C1)C(=O)NC1C(CO)OC(C1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=RTCWNSKNDIMYBP-UHFFFAOYSA-N

Formula

C21H25N7O6

Mass

471.474

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Purine 3'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Purine 3'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine 3'-deoxyribonucleoside - Alpha-amino acid amide - Alanine or derivatives - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Benzyloxycarbonyl - Alpha-amino acid or derivatives - N-substituted-alpha-amino acid - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Imidolactam - Benzenoid - Pyrimidine - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Carbamic acid ester - Tetrahydrofuran - Imidazole - Azole - Secondary carboxylic acid amide - Secondary alcohol - Carbonic acid derivative - Carboxamide group - Amino acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine 3'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 3.

External Descriptors

Not available

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