Structure Information
Structure

Compound Identification

SMILES

CC(=O)NCCCCCCNC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=RWCYUHWDOIKAMW-SCFUHWHPSA-N

Formula

C18H31N6O14P3

Mass

648.395

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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

Not available

Direct Parent

Purine ribonucleoside triphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-alkylaminopurine - 6-aminopurine - Pentose monosaccharide - Monosaccharide phosphate - Imidazopyrimidine - Purine - Monoalkyl phosphate - Aminopyrimidine - Monosaccharide - Pyrimidine - N-substituted imidazole - Phosphoric acid ester - Imidolactam - Organic phosphoric acid derivative - Alkyl phosphate - Acetamide - Azole - Heteroaromatic compound - Oxolane - Imidazole - 1,2-diol - Carboxamide group - Secondary alcohol - Secondary carboxylic acid amide - Organoheterocyclic compound - Oxacycle - Azacycle - Carboxylic acid derivative - Amine - Organic oxide - Carbonyl group - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside triphosphates. These are purine ribobucleotides with a triphosphate group linked to the ribose moiety.

External Descriptors

Not available

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