Structure Information
Structure

Compound Identification

SMILES

NC1=NC2=C(N=CN2[C@H]2[C@@H]3CC[C@H]2C(CO)(CO)C3)C(NC2CC2)=N1

InChIKey

InChIKey=MFXXSLJSYQEIPP-XWIASGKRSA-N

Formula

C17H24N6O2

Mass

344.419

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

Cyclopentyl nucleosides

Intermediate Tree Nodes

1,3-substituted cyclopentyl nucleosides

Direct Parent

1,3-substituted cyclopentyl purine nucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1,3-substituted cyclopentyl purine nucleoside - 6-alkylaminopurine - 6-aminopurine - Aromatic monoterpenoid - Norbornane monoterpenoid - Monoterpenoid - Imidazopyrimidine - Purine - Aminopyrimidine - N-substituted imidazole - Imidolactam - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Primary alcohol - Primary amine - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1,3-substituted cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a hydroxyl group and at the 3-position with either a purine base.

External Descriptors

Not available

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