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Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@H]1CC[C@@H](CO[P+](=O)OC23CCC(CC2)C3)O1

InChIKey

InChIKey=LDDPGFCSTIMTHP-XPFWZQFZSA-N

Formula

C17H23N5O4P

Mass

392.375

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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 2',3'-dideoxyribonucleoside - Purine nucleoside - 6-aminopurine - Aromatic monoterpenoid - Monoterpenoid - Norbornane monoterpenoid - Imidazopyrimidine - Purine - Aminopyrimidine - Imidolactam - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Oxolane - Heteroaromatic compound - Organoheterocyclic compound - Azacycle - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Primary amine - Hydrocarbon derivative - Amine - 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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