Structure Information
Structure

Compound Identification

SMILES

CC(=O)NCC(=O)OP(O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=NC2=C1N=CN=C2N

InChIKey

InChIKey=YAIVSVDFAJFRIL-FRJWGUMJSA-N

Formula

C14H19N6O9P

Mass

446.313

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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 - N-acyl-alpha amino acid or derivatives - N-glycosyl compound - Glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Alpha-amino acid or derivatives - 6-aminopurine - Purine - Imidazopyrimidine - Phosphoethanolamine - Monoalkyl phosphate - Aminopyrimidine - Acyl phosphate - Imidolactam - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Monosaccharide - Heteroaromatic compound - Acetamide - Tetrahydrofuran - Imidazole - Azole - Secondary carboxylic acid amide - Secondary alcohol - Carboxylic acid salt - Carboxamide group - Amino acid or derivatives - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Primary amine - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - 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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