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)OC[C@H]2O[C@H]3NC4=C(N=C3C(=S)[C@H]2S)C(=O)N=C(N)N4)[C@@H](O)[C@H]1O

InChIKey

InChIKey=NZFFQJKPKYYGIT-VOSSIGNKSA-N

Formula

C20H24N10O13P2S2

Mass

738.54

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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 - Pyranopterin - Pentose-5-phosphate - Pentose phosphate - Pterin - N-glycosyl compound - Glycosyl compound - Hypoxanthine - Pentose monosaccharide - Pteridine - Monosaccharide phosphate - 6-oxopurine - Organic pyrophosphate - Imidazopyrimidine - Purine - Monoalkyl phosphate - Aminopyrimidine - Secondary aliphatic/aromatic amine - Pyrimidone - Phosphoric acid ester - Oxane - Alkyl phosphate - Monosaccharide - N-substituted imidazole - Pyrimidine - Organic phosphoric acid derivative - Heteroaromatic compound - Imidazole - Oxolane - Azole - Vinylogous amide - 1,2-diol - Ketimine - Thioketone - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Secondary amine - Alkylthiol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary amine - Hydrocarbon derivative - Organic oxide - Imine - Organic nitrogen compound - Amine - Alcohol - Thiocarbonyl group - Organic oxygen compound - 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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