Compound Identification
SMILES
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1\C=C\C=C(Br)Br)N1C=CC(=O)NC1=O
InChIKey
InChIKey=IAGTUTZVQCCHLE-LTEIFJFTSA-N
Formula
C12H12Br2N2O5
Mass
424.045
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
- Class 5'-deoxyribonucleosides
-
Superclass
Nucleosides, nucleotides, and analogues
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
Glycosylamines Pyrimidones Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Lactams Ketene acetals 1,2-diols Ureas Secondary alcohols Oxacyclic compounds Vinyl bromides Azacyclic compounds Bromoalkenes Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pyrimidone - Hydropyrimidine - Pyrimidine - Oxolane - Heteroaromatic compound - Vinylogous amide - 1,2-diol - Ketene acetal or derivatives - Lactam - Secondary alcohol - Urea - Haloalkene - Organoheterocyclic compound - Azacycle - Oxacycle - Bromoalkene - Vinyl halide - Vinyl bromide - Organic oxygen compound - Organobromide - Organohalogen compound - Alcohol - Organic oxide - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteromonocyclic 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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