Structure Information
Structure

Compound Identification

SMILES

O[C@@H]1[C@@H](C[Se])O[C@H]([C@@H]1O)N1C=NC2=C(CC3=CC=C(C=C3)[N+]([O-])=O)N=CN=C12

InChIKey

InChIKey=ZVKDGPVRWITUFR-DNNBLBMLSA-N

Formula

C17H16N5O5Se

Mass

449.316

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

5'-deoxyribonucleosides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

5'-deoxyribonucleosides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Imidazopyrimidine - Nitrobenzene - Purine - Nitroaromatic compound - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Heteroaromatic compound - Imidazole - Oxolane - Azole - Organic nitro compound - C-nitro compound - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Alcohol - Organopnictogen compound - Organic salt - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organoselenium compound - Organic zwitterion - Hydrocarbon derivative - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

External Descriptors

Not available

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