Structure Information
Structure

Compound Identification

SMILES

NC1=C2N=CN([C@@H]3O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]3O)C2N(NCCCCCCNC(=O)CCCC[C@@H]2SC[C@@H]3NC(=O)N[C@H]23)C=N1

InChIKey

InChIKey=HUEGRJQJZDVOAA-SFEANKRVSA-N

Formula

C26H46N9O15P3S

Mass

849.68

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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

Aliphatic heteropolycyclic compounds

Substituents

Purine ribonucleoside triphosphate - Biotin_derivative - Pentose phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Imidazopyrimidine - Thienoimidazolidine - Monoalkyl phosphate - Fatty amide - Phosphoric acid ester - Organic phosphoric acid derivative - N-acyl-amine - Monosaccharide - Imidazolidinone - Alkyl phosphate - 1,6-dihydropyrimidine - Hydropyrimidine - Fatty acyl - Oxolane - 2-imidazoline - Thiolane - Imidazolidine - Thiophene - Carboxylic acid amidrazone - Carboxamide group - 1,2-diol - Urea - Secondary carboxylic acid amide - Secondary alcohol - Formamidine - Carboxylic acid amidine - Oxacycle - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Dialkylthioether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Thioether - Amidine - Alcohol - Amine - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Aliphatic 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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