Structure Information
Structure

Compound Identification

SMILES

O[C@H]1[C@H](CO[P+](=O)O[P+](=O)O[P+](=O)O[P+](=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(=O)NC2=O)O[C@@H]([C@H]1O)N1C=NC2=C1NC(=O)NC2=O

InChIKey

InChIKey=MYGDMLGKTFKJOD-DLZVHFHUSA-Q

Formula

C19H22N6O19P4

Mass

762.301

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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 heteropolycyclic compounds

Substituents

Purine ribonucleoside phosphonate - Purine nucleoside - Pyrimidine nucleoside - Glycosyl compound - N-glycosyl compound - Xanthine - 6-oxopurine - Purinone - Imidazopyrimidine - Purine - Alkaloid or derivatives - Pyrimidone - Pyrimidine - Hydropyrimidine - Monosaccharide - N-substituted imidazole - Vinylogous amide - Azole - Heteroaromatic compound - Imidazole - Oxolane - Urea - Secondary alcohol - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen 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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