Structure Information
Structure

Compound Identification

SMILES

CC1(O)C(O)C(COP(O)(=O)OP(O)(O)=O)OC1N1C=C(C#CC2=CC=NC=C2)C2=C1N=CN=C2N

InChIKey

InChIKey=URQCQFAEWDMQTG-UHFFFAOYSA-N

Formula

C19H21N5O10P2

Mass

541.35

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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 - Monosaccharide phosphate - Organic pyrophosphate - Pentose monosaccharide - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Monoalkyl phosphate - Monosaccharide - Organic phosphoric acid derivative - Phosphoric acid ester - Pyridine - Pyrimidine - Imidolactam - Substituted pyrrole - Alkyl phosphate - Tertiary alcohol - Oxolane - Pyrrole - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organoheterocyclic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organic oxygen compound - Amine - Organic oxide - Primary amine - 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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