Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1C(O)C=C(CO[P+](=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(N)=NC2=O)OC1[C@@H](O)[C@@H](O)CO

InChIKey

InChIKey=AWACKXLBBLERFK-FZXFPNARSA-O

Formula

C20H30N4O13P

Mass

565.448

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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

Aromatic heteromonocyclic compounds

Substituents

Purine ribonucleoside phosphonate - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Aminopyrimidine - Pyrimidone - Hydropyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Heteroaromatic compound - Oxolane - Acetamide - Secondary alcohol - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Polyol - Carboxylic acid derivative - Amine - Primary amine - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Alcohol - Carbonyl group - Organic nitrogen compound - Primary alcohol - Organic cation - Aromatic heteromonocyclic 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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