Compound Identification
SMILES
CC(=O)OC[C@@H]1O[C@@H]([C@@H](OC(C)=O)[C@H]1OC(C)=O)N1C=NC2=C1C(=O)N=C(Br)N2
InChIKey
InChIKey=DYSUQXLQPPCSST-OXUWNYNTSA-N
Formula
C16H17BrN4O8
Mass
473.236
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Nucleoside and nucleotide analogues
Alternative Parents
Glycosylamines 6-oxopurines Hypoxanthines Tricarboxylic acids and derivatives Pyrimidones 2-halopyrimidines Aryl bromides N-substituted imidazoles Monosaccharides Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Carboxylic acid esters Oxacyclic compounds Azacyclic compounds Organic oxides Organobromides Carbonyl compounds Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Tricarboxylic acid or derivatives - Purine - 2-halopyrimidine - Halopyrimidine - Pyrimidone - Aryl bromide - Aryl halide - N-substituted imidazole - Monosaccharide - Pyrimidine - Azole - Tetrahydrofuran - Vinylogous amide - Imidazole - Heteroaromatic compound - Carboxylic acid ester - Carboxylic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as nucleoside and nucleotide analogues. These are analogues of nucleosides and nucleotides. These include phosphonated nucleosides, C-glycosylated nucleoside bases, analogues where the sugar unit is a pyranose, and carbocyclic nucleosides, among others.
External Descriptors
Not available