Structure Information
Structure

Compound Identification

SMILES

COCC1OC(C(OC)C1OC)N1C=C(CN(C2C=CC(OC)C2OC)C(C)=O)C2=C1N=C(N=C2OC)N(C)C

InChIKey

InChIKey=CVZGOKIZJBSQOL-UHFFFAOYSA-N

Formula

C27H41N5O8

Mass

563.652

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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 - Pyrrolopyrimidine - Pyrrolo[2,3-d]pyrimidine - Dialkylarylamine - Aminopyrimidine - Alkyl aryl ether - Monosaccharide - Pyrimidine - Substituted pyrrole - Heteroaromatic compound - Acetamide - Tetrahydrofuran - Tertiary carboxylic acid amide - Pyrrole - Carboxamide group - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Hydrocarbon derivative - 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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