Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1CC(COP(O)(O)=O)C(O)C1O

InChIKey

InChIKey=ZLHJFTIXCUYZSQ-UHFFFAOYSA-N

Formula

C11H16N5O6P

Mass

345.252

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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-aminopurine - Imidazopyrimidine - Purine - Monoalkyl phosphate - Aminopyrimidine - Cyclopentanol - Imidolactam - Alkyl phosphate - Pyrimidine - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Cyclic alcohol - Heteroaromatic compound - Imidazole - Azole - 1,2-diol - Secondary alcohol - Azacycle - Organoheterocyclic compound - Primary amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Amine - Alcohol - Organooxygen compound - Organonitrogen compound - 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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