Compound Identification
SMILES
O[C@H]1[C@H](O)[C@@H](O[C@@H]1CN=[N+]=[N-])N1C=C(Br)C(=O)NC1=O
InChIKey
InChIKey=MYHKQVDCHSQMHC-MNCSTQPFSA-N
Formula
C9H10BrN5O5
Mass
348.113
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 Pentoses Halopyrimidines Pyrimidones Aryl bromides Hydropyrimidines Vinylogous amides Heteroaromatic compounds Oxolanes Lactams 1,2-diols Secondary alcohols Ureas Azo imides Azo compounds Azacyclic compounds Oxacyclic compounds Organic salts Organic oxides Hydrocarbon derivatives Organic zwitterions Organobromides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Halopyrimidine - Pyrimidone - Aryl bromide - Aryl halide - Hydropyrimidine - Monosaccharide - Pyrimidine - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary alcohol - Azo compound - Azo imide - 1,2-diol - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Organic salt - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Organic zwitterion - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Organobromide - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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