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](O)C(=S)C(=S)C2=CNC3=C(N2)C(=O)N=C(N)N3)[C@@H](O)[C@H]1O

InChIKey

InChIKey=MNEQOJMCKOBWNR-QKVCZYCRSA-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 - Pentose phosphate - Pentose-5-phosphate - Pterin - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Pteridine - Imidazopyrimidine - Purine - Pyrimidone - Aminopyrimidine - Monoalkyl phosphate - Pyrimidine - Monosaccharide - Alkyl phosphate - N-substituted imidazole - Phosphoric acid ester - Organic phosphoric acid derivative - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Oxolane - Secondary alcohol - Thioketone - 1,2-diol - Organoheterocyclic compound - Oxacycle - Azacycle - Enamine - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alcohol - Primary amine - Organooxygen compound - Organosulfur compound - Thiocarbonyl group - 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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