Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OCCC[N+]2=CC=C(C=C2)C(=O)CBr)[C@@H](O)[C@H]1O

InChIKey

InChIKey=TVGJSGTUHNIVQU-WVSUBDOOSA-O

Formula

C20H26BrN6O11P2

Mass

668.31

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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 diphosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside diphosphate - Purine ribonucleoside monophosphate - Pentose-5-phosphate - Pentose phosphate - Organic pyrophosphate - Imidazopyrimidine - Aryl alkyl ketone - Aryl ketone - Hydroxypyridine - Imidolactam - Alpha-branched alpha,beta-unsaturated-ketone - Alkyl phosphate - Pyrimidine - Pyridine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Monosaccharide - Alpha-haloketone - Heteroaromatic compound - Alpha,beta-unsaturated ketone - Tetrahydrofuran - Enone - Azole - Acryloyl-group - Secondary alcohol - Ketone - Formamidine - Oxacycle - Azacycle - Organoheterocyclic compound - Carboximidamide - Amidine - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Amine - Alkyl halide - Alkyl bromide - Alcohol - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside diphosphates. These are purine ribobucleotides with diphosphate group linked to the ribose moiety.

External Descriptors

Not available

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