Structure Information
Structure

Compound Identification

SMILES

C[C@@]1(O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(O)=O)O[C@H]1N1C=C(C#CC(O)=O)C2=C1N=CN=C2N

InChIKey

InChIKey=DLDGBVYXHIIKJX-ZCLWBALQSA-N

Formula

C15H18N4O12P2

Mass

508.273

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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 phosphate - Pentose-5-phosphate - Glycosyl compound - N-glycosyl compound - Organic pyrophosphate - Monosaccharide phosphate - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Monoalkyl phosphate - Phosphoric acid ester - Primary aromatic amine - Pyrimidine - Substituted pyrrole - Alkyl phosphate - Monosaccharide - Organic phosphoric acid derivative - Imidolactam - Heteroaromatic compound - Oxolane - Tertiary alcohol - Pyrrole - Secondary alcohol - Amino acid - 1,2-diol - Amino acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Oxacycle - Azacycle - Organoheterocyclic compound - Amine - Hydrocarbon derivative - Organic oxide - Alcohol - Organic nitrogen compound - Carbonyl group - Organic oxygen compound - Organopnictogen compound - Primary amine - Organonitrogen compound - Organooxygen 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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