Structure Information
Structure

Compound Identification

SMILES

CCN(CC)C1=C(C=C(C=NNC2=NC3=C(NC(N)=NC3=O)N2C2OC(CO)C(O)C2O)C=C1)[N+]([O-])=O

InChIKey

InChIKey=FPYAHQKKNJGSMS-UHFFFAOYSA-N

Formula

C21H27N9O7

Mass

517.503

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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 - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Nitrobenzene - Purine - Dialkylarylamine - Aniline or substituted anilines - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Aminopyrimidine - Pyrimidone - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Benzenoid - Pyrimidine - Vinylogous amide - Azole - Imidazole - Oxolane - Heteroaromatic compound - Secondary alcohol - Tertiary amine - Organic nitro compound - C-nitro compound - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Hydrazone - Organic oxoazanium - Organoheterocyclic compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Primary amine - Organic nitrogen compound - Alcohol - Organic oxide - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organic salt - Hydrocarbon derivative - Amine - Primary alcohol - Organic zwitterion - 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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