Structure Information
Structure

Compound Identification

SMILES

CP(O)(=O)OP(C)(=O)OP(C)(=O)OCC1OC(C(O)C1O)N1C=C(C2=CSC=C2)C2=C1N=CN=C2N

InChIKey

InChIKey=RPRDBUWXAWAKIO-UHFFFAOYSA-N

Formula

C18H25N4O10P3S

Mass

582.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrrolopyrimidine nucleosides and nucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Pyrrolopyrimidine nucleosides and nucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Pyrrolopyrimidine ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Monosaccharide - Phosphonic acid ester - Pyrimidine - Imidolactam - Substituted pyrrole - Organophosphonic acid - Organophosphonic acid derivative - Oxolane - Heteroaromatic compound - Pyrrole - Thiophene - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Primary amine - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as pyrrolopyrimidine nucleosides and nucleotides. These are nucleoside derivatives containing a ribose derivative which is n-glycosylated to a pyrrolopyrimidine. Also called deazapurine nucleosides, they are analogs of purine nucleosides with the N atom of the purine being replaced by a C atom at position 7.

External Descriptors

Not available

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