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Structure Information
Structure

Compound Identification

SMILES

NC1=NC(Cl)=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](CO)O1.CC1=CN([C@@H]2O[C@H](CO[P+](O)=O)C[C@H]2O)C(=O)NC1=O

InChIKey

InChIKey=GGVRLGOHWCFTSG-QFYOUVLZSA-P

Formula

C20H26ClN7O10P

Mass

590.89

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Deoxyribo- and ribonucleoside phosphonates

Subclass

Purine ribonucleoside phosphonates

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside phosphonates

Alternative Parents

Molecular Framework

Not available

Substituents

Purine ribonucleoside phosphonate - Purine 2'-deoxyribonucleoside - Purine nucleoside - Pyrimidine 3'-deoxyribonucleoside - Pyrimidine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Pyrimidone - Aryl chloride - Aryl halide - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Urea - Secondary alcohol - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Primary alcohol - Hydrocarbon derivative - Amine - Organic oxide - Alcohol - Primary amine - Organic nitrogen compound - Organooxygen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside phosphonates. These are n-glycosyl compound that possess both a purine nucleobase linked to either a ribose or deoxyribose, which in turn carries a phosphonate group at the 5'-position.

External Descriptors

Not available

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