Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=C(SC1=CC=CC=C1)N2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=DCARDSHKJRCYNY-SDBHATRESA-N

Formula

C16H20N5O13P3S

Mass

615.34

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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 - Diarylthioether - 6-aminopurine - Monosaccharide phosphate - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Thiophenol ether - Aminopyrimidine - Monoalkyl phosphate - Alkyl phosphate - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Benzenoid - Pyrimidine - Oxolane - Azole - Heteroaromatic compound - Imidazole - Secondary alcohol - 1,2-diol - Azacycle - Oxacycle - Thioether - Sulfenyl compound - Organoheterocyclic compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Alcohol - Primary amine - Amine - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organooxygen 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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