Structure Information
Structure

Compound Identification

SMILES

OCC1OC(C(O)C1O)N1C=C(C#N)C2=C1N=CN=C2[Se]CC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=XVRFNXZGRPAATC-UHFFFAOYSA-N

Formula

C19H17N5O6Se

Mass

490.345

Export to:

JSON SDF CSV

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 - Nitrobenzene - Pyrrolo[2,3-d]pyrimidine - Nitroaromatic compound - Substituted pyrrole - Pyrimidine - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Heteroaromatic compound - Pyrrole - Tetrahydrofuran - Organic nitro compound - Secondary alcohol - C-nitro compound - Carbonitrile - Nitrile - Oxacycle - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Selenoether - Organonitrogen compound - Organic oxygen compound - Organooxygen compound - Organoselenium compound - Organopnictogen compound - Primary alcohol - Organic oxide - Alcohol - Hydrocarbon derivative - Organic nitrogen compound - Organic zwitterion - 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

Previous Back Next