Structure Information
Structure

Compound Identification

SMILES

COC(=O)C(CC1=CNC2=CC=CC=C12)NP(O)(=O)OCC1OC(C(O)C1O)N1C=CC2=C1N=CN=C2N

InChIKey

InChIKey=OORXODSIUNMKHH-UHFFFAOYSA-N

Formula

C23H27N6O8P

Mass

546.477

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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 - Alpha-amino acid ester - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - Pentose monosaccharide - 3-alkylindole - Pyrrolo[2,3-d]pyrimidine - Indole - Indole or derivatives - Pyrrolopyrimidine - Aminopyrimidine - Fatty acid ester - Phosphoric monoester monoamide - Monosaccharide - Organic phosphoric acid derivative - Imidolactam - Phosphoric acid ester - Organic phosphoric acid amide - Pyrimidine - Fatty acyl - Substituted pyrrole - Benzenoid - Oxolane - Pyrrole - Methyl ester - Heteroaromatic compound - 1,2-diol - Secondary alcohol - Amino acid or derivatives - Carboxylic acid ester - Oxacycle - Monocarboxylic acid or derivatives - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Primary amine - Alcohol - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organonitrogen compound - Amine - Organic oxygen compound - Organooxygen compound - Organic nitrogen 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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