Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OC(=O)[C@@H]2CCCN2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=KQFKHTAASHMYDJ-TWBCTODHSA-N

Formula

C15H21N6O8P

Mass

444.341

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