Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1[C@H](OP(=O)(NCCCCCC(O)=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=CC(N)=CC2=O)[C@@H](COP(O)(O)=O)O[C@H]1N1C=CC2=C1NC(N)=NC2=O

InChIKey

InChIKey=NJUAYRKYMUBUAI-PQBCODKWSA-N

Formula

C28H41N7O16P2

Mass

793.617

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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 - N-glycosyl compound - Glycosyl compound - Monosaccharide phosphate - Pyrrolo[2,3-d]pyrimidine - Pyrrolopyrimidine - Medium-chain fatty acid - Phosphoric diester monoamide - Monoalkyl phosphate - Hydroxy fatty acid - Aminopyrimidine - Pyridinone - Pyrimidone - Aminopyridine - Dihydropyridine - Hydropyridine - Monosaccharide - Organic phosphoric acid derivative - Fatty acyl - Phosphoric acid ester - Pyridine - Fatty acid - Pyrimidine - Substituted pyrrole - Organic phosphoric acid amide - Alkyl phosphate - Pyrrole - Oxolane - Heteroaromatic compound - Vinylogous amide - Amino acid - Amino acid or derivatives - 1,2-diol - Secondary alcohol - Lactam - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid derivative - Carboxylic acid - Azacycle - Dialkyl ether - Ether - Organoheterocyclic compound - Organic nitrogen compound - Primary amine - Organic oxygen compound - Carbonyl group - Organic oxide - Hydrocarbon derivative - Alcohol - 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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