Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2N=NC3=C2C=CC(=C3)[N+]([O-])=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=DRZCRPWRMXVXPD-PLEFRAQWSA-N

Formula

C21H25N9O15P2

Mass

705.427

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Subclass

Purine nucleotide sugars

Intermediate Tree Nodes

Not available

Direct Parent

Purine nucleotide sugars

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine nucleotide sugar - Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - 1-ribofuranosylbenzotriazole - Pentose-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Organic pyrophosphate - 6-aminopurine - Monosaccharide phosphate - Purine - Benzotriazole - Imidazopyrimidine - Nitroaromatic compound - Monoalkyl phosphate - Aminopyrimidine - Monosaccharide - N-substituted imidazole - Organic phosphoric acid derivative - Imidolactam - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Benzenoid - Azole - 1,2,3-triazole - Triazole - Heteroaromatic compound - Imidazole - Oxolane - Secondary alcohol - 1,2-diol - C-nitro compound - Organic nitro compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organic oxoazanium - Organic oxide - Amine - Organic oxygen compound - Hydrocarbon derivative - Organic zwitterion - Organic salt - Primary amine - Organic nitrogen compound - Organooxygen compound - Alcohol - Organonitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.

External Descriptors

Not available

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