Structure Information
Structure

Compound Identification

SMILES

[H]C1(COP(O)(=O)OC(=O)CCC)OC([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])O

InChIKey

InChIKey=HXYASMGHIVHQEN-MEKHUTDWSA-N

Formula

C14H20N5O8P

Mass

417.315

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