Structure Information
Structure

Compound Identification

SMILES

CSC1=NC2=C(N=CN2[C@@H]2O[C@H](COP(O)(=O)C(Cl)(Cl)P(O)(=O)C(Cl)(Cl)P(O)(O)=O)[C@@H](O)[C@H]2O)C(N)=N1

InChIKey

InChIKey=MXJLXBYQBDOAGZ-KQYNXXCUSA-N

Formula

C13H18Cl4N5O11P3S

Mass

687.09

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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 monophosphates

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Purine ribonucleoside monophosphate - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Pentose monosaccharide - Imidazopyrimidine - Purine - Aryl thioether - Aminopyrimidine - Alkylarylthioether - Monosaccharide - N-substituted imidazole - Imidolactam - Phosphonic acid ester - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Organophosphonic acid - Organophosphonic acid derivative - Oxolane - Secondary alcohol - 1,2-diol - Thioether - Sulfenyl compound - Organoheterocyclic compound - Oxacycle - Azacycle - Organosulfur compound - Organohalogen compound - Alkyl chloride - Alkyl halide - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organochloride - Organic oxygen compound - Amine - Organonitrogen compound - Organooxygen compound - Primary amine - Organophosphorus compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.

External Descriptors

Not available

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