Structure Information
Structure

Compound Identification

SMILES

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

InChIKey

InChIKey=GDPVENOGSVMRJL-FSRKKXLISA-N

Formula

C16H24N5O10P

Mass

477.367

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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 - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - Acyl phosphate - Monoalkyl phosphate - Organic phosphoric acid derivative - N-substituted imidazole - Phosphoric acid ester - Monosaccharide - Alkyl phosphate - Pyrimidine - Imidolactam - Azole - Imidazole - Tetrahydrofuran - Heteroaromatic compound - Amino acid or derivatives - Carboxylic acid salt - Secondary alcohol - Oxacycle - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Organooxygen compound - Organic salt - Alcohol - Primary amine - Organic oxide - Primary alcohol - Carbonyl group - Organic oxygen compound - Hydrocarbon derivative - Organopnictogen compound - Amine - Organic nitrogen 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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