Structure Information
Structure

Compound Identification

SMILES

NC1=NC(F)=NC2=C1N=CN2[C@H]1O[C@@H](COP(O)(=O)OP(O)(O)=O)[C@H](O)[C@H]1O

InChIKey

InChIKey=ZAHBDWMZWHJOLZ-HJGQOHIQSA-N

Formula

C10H14FN5O10P2

Mass

445.193

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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 diphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Monoalkyl phosphate - Aryl fluoride - Aryl halide - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Azole - Oxolane - Heteroaromatic compound - Imidazole - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Organofluoride - Alcohol - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Amine - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Primary amine - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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