Structure Information
Structure

Compound Identification

SMILES

NC1=NC(=O)C2=C(N1)N(C=N2)[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OCCCCC(=O)NC(CC2=CC=CC=C2)C2=CC=CC=C2)[C@@H](O)[C@H]1O

InChIKey

InChIKey=PXERNESXFNAFNV-DGPRTRQTSA-N

Formula

C29H36N6O12P2

Mass

722.585

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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 - Stilbene glycoside - Purine ribonucleoside monophosphate - Pentose-5-phosphate - Pentose phosphate - Stilbene - N-glycosyl compound - Glycosyl compound - Hypoxanthine - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Amphetamine or derivatives - 6-oxopurine - Imidazopyrimidine - Purine - Pyrimidone - Monoalkyl phosphate - Aminopyrimidine - Monocyclic benzene moiety - Fatty amide - Fatty acyl - Monosaccharide - N-acyl-amine - N-substituted imidazole - Organic phosphoric acid derivative - Benzenoid - Alkyl phosphate - Phosphoric acid ester - Pyrimidine - Azole - Vinylogous amide - Oxolane - Imidazole - Heteroaromatic compound - Secondary alcohol - Secondary carboxylic acid amide - 1,2-diol - Amino acid or derivatives - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Alcohol - Amine - Organic oxygen compound - Organic oxide - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - 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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