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[C@H]3C(=S)C2S)C(=O)N=C(N)N4)[C@@H](O)[C@H]1O

InChIKey

InChIKey=UXPZVMWSOYLZFA-YOSJPQBZSA-N

Formula

C20H26N10O13P2S2

Mass

740.55

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