Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[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-])(=S)O[C@@H]4[C@H](O)[C@@H](CO)O[C@H]4N4C=NC5=C4N=CN=C5N)O[C@H]3N3C=NC4=C3N=CN=C4N)O[C@H]2N2C=NC3=C2N=CN=C3N)[C@@H](O)[C@H]1O

InChIKey

InChIKey=WFBXAZQJVVUYMY-QXFQXOIWSA-K

Formula

C40H46N20O21P3S

Mass

1267.91

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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

Purine ribonucleoside bisphosphates

Direct Parent

Purine ribonucleoside 2',5'-bisphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside 2',5'-bisphosphate - Purine ribonucleoside monophosphate - Pentose-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Dialkyl phosphate - Aminopyrimidine - Thiophosphoric acid ester - Imidolactam - Organic phosphoric acid derivative - Organic thiophosphoric acid or derivatives - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Tetrahydrofuran - Secondary alcohol - Organoheterocyclic compound - Oxacycle - Azacycle - Organic nitrogen compound - Alcohol - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Amine - Organic anion - Aromatic heteropolycyclic compound

Description

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

External Descriptors

Not available

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