Structure Information
Structure

Compound Identification

SMILES

CCNC(=O)C1OC(C(O)C1O)N1C=NC2=C1N=CN=C2NCC1=CC=CC=C1[N+]([O-])=O

InChIKey

InChIKey=CZZHLXAEYDPEMY-UHFFFAOYSA-N

Formula

C19H21N7O6

Mass

443.42

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleoside - 6-alkylaminopurine - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Nitrobenzene - Purine - Imidazopyrimidine - Nitroaromatic compound - Benzylamine - Aminopyrimidine - Secondary aliphatic/aromatic amine - Monocyclic benzene moiety - Benzenoid - N-substituted imidazole - Pyrimidine - Imidolactam - Imidazole - Azole - Heteroaromatic compound - Oxolane - Organic nitro compound - Secondary carboxylic acid amide - C-nitro compound - Secondary alcohol - 1,2-diol - Amino acid or derivatives - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Secondary amine - Organic oxoazanium - Organic salt - Carbonyl group - Alcohol - Amine - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

External Descriptors

Not available

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