Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OC(=O)C2CS\C(N2)=C2/OC3=CC(=O)C=CC3=C2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=RQAWMLVHKPRFEF-XORXNVDESA-N

Formula

C22H21N6O10PS

Mass

592.48

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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 monophosphates

Direct Parent

5'-acylphosphoadenosines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-acylphosphoadenosine - Pentose phosphate - Pentose-5-phosphate - N-glycosyl compound - Glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Benzofuran - Purine - Monoalkyl phosphate - Acyl phosphate - Aminopyrimidine - Alkyl phosphate - Imidolactam - Pyrimidine - Monosaccharide - Phosphoric acid ester - N-substituted imidazole - Organic phosphoric acid derivative - Thiazolidine - Imidazole - Azole - Heteroaromatic compound - Furan - Oxolane - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Ketone - Cyclic ketone - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Primary amine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Carbonyl group - Alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-acylphosphoadenosines. These are ribonucleoside derivatives containing an adenoside moiety, where the phosphate group is acylated.

External Descriptors

Not available

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