Structure Information
Structure

Compound Identification

SMILES

NC1=NC=NC2=C1C=CN2[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O

InChIKey

InChIKey=OBKZXEICLJXEAO-KCGFPETGSA-N

Formula

C11H15N4O7P

Mass

346.236

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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-5-phosphate - Pentose phosphate - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Monosaccharide phosphate - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Aminopyrimidine - Monoalkyl phosphate - Pyrimidine - Imidolactam - Alkyl phosphate - Phosphoric acid ester - Substituted pyrrole - Organic phosphoric acid derivative - Monosaccharide - Heteroaromatic compound - Tetrahydrofuran - Pyrrole - 1,2-diol - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Primary amine - 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

CHEBI:74555 : ribonucleoside 5'-monophosphate

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