Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@]3([C@H](O)[C@@H]2O)N2C=C(CC=C32)C(O)=O)O[C@@H]([C@@H]1OP(O)(O)=O)N1C=NC2=C1N=CN=C2N1OO1

InChIKey

InChIKey=AWCVLMXGQCACJU-QEZJJQCUSA-N

Formula

C21H25N6O20P3

Mass

774.374

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleotide sugar - Purine ribonucleoside 2',5'-bisphosphate - Purine ribonucleoside bisphosphate - Purine ribonucleoside diphosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Organic pyrophosphate - Imidazopyrimidine - Purine - Azepine - Dihydropyridine - Monoalkyl phosphate - Alkyl phosphate - Monosaccharide - N-substituted imidazole - Pyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - N-vinylaziridine - Azole - Vinylaziridine - Imidazole - Vinylogous amide - Tetrahydrofuran - Heteroaromatic compound - Secondary alcohol - Carboxylic acid - Oxacycle - Enamine - Aziridine - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Azacycle - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Alcohol - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Carbonyl group - Organopnictogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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