Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1OC1=C(C=C(C=C1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O

InChIKey

InChIKey=LAJOACNWQUUFTP-UHFFFAOYSA-N

Formula

C16H17N8O19P3

Mass

718.27

Export to:

JSON SDF CSV

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-5-phosphate - Pentose phosphate - Nitrophenyl ether - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Monosaccharide phosphate - Purine - Imidazopyrimidine - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Alkyl aryl ether - Monoalkyl phosphate - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Phosphoric acid ester - Primary aromatic amine - Pyrimidine - Alkyl phosphate - Benzenoid - Oxolane - Azole - Imidazole - Heteroaromatic compound - Secondary alcohol - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Ether - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxoazanium - Azacycle - Oxacycle - Organic oxide - Alcohol - Organic oxygen compound - Hydrocarbon derivative - Amine - Organic salt - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organopnictogen compound - Primary amine - Organic zwitterion - 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

Previous Back Next