Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OC(=O)CCCC[C@@H]2CCSS2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=QWEGOCJRZOKSOE-ADUAKINBSA-N

Formula

C18H26N5O8PS2

Mass

535.53

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

CHEBI:83864 : lipoyl-AMP

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