Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)O[C@@H]2[C@H](O)[C@@H](COP(O)(=O)O[C@@H]3[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]3N3C=NC4=C3N=CN=C4N)O[C@H]2N2C=NC3=C2N=CN=C3N)[C@](O)(F)[C@H]1O

InChIKey

InChIKey=XSZQRCKQMAJEOT-ALOUAQMWSA-N

Formula

C30H39FN15O25P5

Mass

1183.589

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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 2',5'-bisphosphate - Purine ribonucleoside bisphosphate - Purine ribonucleoside monophosphate - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Imidazopyrimidine - Purine - Aminopyrimidine - Dialkyl phosphate - Monoalkyl phosphate - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Imidolactam - Alkyl phosphate - Pyrimidine - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Fluorohydrin - Halohydrin - Azacycle - Organoheterocyclic compound - Oxacycle - Organohalogen compound - Alkyl fluoride - Organofluoride - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Alkyl halide - Primary amine - Amine - Organic oxygen compound - Organic nitrogen compound - Alcohol - 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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