Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CC(OP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChIKey

InChIKey=CNUZICGKLOTDRJ-ZYCSGJNZSA-N

Formula

C20H27N10O16P3

Mass

756.411

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine ribonucleotides

Intermediate Tree Nodes

Not available

Direct Parent

Purine ribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Purine ribonucleoside monophosphate - 5'-deoxyribonucleoside - Disaccharide phosphate - Disaccharide - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Organic phosphoric acid derivative - N-substituted imidazole - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Heteroaromatic compound - Oxolane - Azole - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.

External Descriptors

Not available

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