Compound Identification
SMILES
OC1C(O)C(OC1CF)N1C=C(Br)C(=O)NC1=O
InChIKey
InChIKey=ONUVAOQZEVZTLW-UHFFFAOYSA-N
Formula
C9H10BrFN2O5
Mass
325.09
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 Azacyclic compounds Oxacyclic compounds Organobromides Organic oxides Hydrocarbon derivatives Alkyl fluorides Organofluorides Organonitrogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Pyrimidone - Halopyrimidine - Monosaccharide - Pyrimidine - Aryl bromide - Hydropyrimidine - Aryl halide - Oxolane - Vinylogous amide - Heteroaromatic compound - Secondary alcohol - Urea - 1,2-diol - Lactam - Oxacycle - Azacycle - Organoheterocyclic compound - Organonitrogen compound - Organooxygen compound - Alkyl fluoride - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Organohalogen compound - Organobromide - Organofluoride - 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 These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom.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