Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)N(C=C1)C1O[C@H](COP(O)(=O)O[C@@H]2[C@H](O)[C@@H](COP(O)(=O)O[C@@H]3[C@H](O)[C@@H](COP(O)(O)=O)OC3N3C=CC(N)=NC3=O)OC2N2C=CC(N)=NC2=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=PUUREYJQAGDFSL-JRXXYSHDSA-N

Formula

C27H38N9O22P3

Mass

933.563

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleotides

Subclass

Pyrimidine ribonucleotides

Intermediate Tree Nodes

Pyrimidine ribonucleoside bisphosphates

Direct Parent

Pyrimidine ribonucleoside 2',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine ribonucleoside 2',5'-bisphosphate - Pyrimidine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Aminopyrimidine - Pyrimidone - Monoalkyl phosphate - Dialkyl phosphate - Alkyl phosphate - Pyrimidine - Imidolactam - Phosphoric acid ester - Hydropyrimidine - Monosaccharide - Organic phosphoric acid derivative - Heteroaromatic compound - Oxolane - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organonitrogen compound - Organic oxide - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Primary amine - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine ribonucleoside 2',5'-bisphosphates. These are pyrimidine ribobucleotides with one phosphate group attached to 2' and 5' hydroxyl groups of the ribose moiety.

External Descriptors

Not available

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