Structure Information
Structure

Compound Identification

SMILES

CSC1=NC=NC2=C1C=CN2C1OC(COP(O)(O)=O)C(O)C1O

InChIKey

InChIKey=RDLNVHQUQZBWDF-UHFFFAOYSA-N

Formula

C12H16N3O7PS

Mass

377.31

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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 - Pentose-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Monosaccharide phosphate - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - Aryl thioether - Monoalkyl phosphate - Alkylarylthioether - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Monosaccharide - Substituted pyrrole - Pyrimidine - Heteroaromatic compound - Pyrrole - Oxolane - Secondary alcohol - 1,2-diol - Oxacycle - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic oxide - 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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