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Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=HNBLQRUAHHCFDI-YVLZZHOMSA-N

Formula

C18H26N5O9P

Mass

487.406

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