Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=NC=NC2=C1C(=CN2C1OC(COC(C)=O)C(OC(C)=O)C1OC(C)=O)C(N)=O

InChIKey

InChIKey=JHJRENZMYFNCTB-UHFFFAOYSA-N

Formula

C20H23N5O9

Mass

477.43

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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 - Pyrrolopyrimidine - N-acetylarylamine - Pyrrolo[2,3-d]pyrimidine - Tricarboxylic acid or derivatives - Pyrrole-3-carboxylic acid or derivatives - N-arylamide - Pyrrole-3-carboxamide - Substituted pyrrole - Monosaccharide - Imidolactam - Pyrimidine - Heteroaromatic compound - Pyrrole - Tetrahydrofuran - Vinylogous amide - Acetamide - Primary carboxylic acid amide - Carboxamide group - Carboxylic acid ester - Secondary carboxylic acid amide - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Carbonyl group - 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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