Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](OC2=C(C=C(C=C2[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O)[C@H]1O

InChIKey

InChIKey=ZKQRAGPWYWGJRD-NZLORHDLSA-N

Formula

C16H17N8O19P3

Mass

718.27

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