Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@H]1O)N1C(Br)=NC(Br)=C1Br
InChIKey
InChIKey=PFIVYLCJNNMZQJ-PAMHENJLSA-N
Formula
C8H9Br3N2O4
Mass
436.882
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Imidazole ribonucleosides and ribonucleotides
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Imidazole ribonucleosides and ribonucleotides
Alternative Parents
Glycosylamines Pentoses 1,2,4,5-tetrasubstituted imidazoles N-substituted imidazoles Aryl bromides Oxolanes Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Organobromides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Imidazole ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 1,2,4,5-tetrasubstituted imidazole - Aryl bromide - Aryl halide - Monosaccharide - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Oxolane - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Organobromide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as imidazole ribonucleosides and ribonucleotides. These are organic compounds in which the C-1 of a ribosyl moiety is N-linked to an imidazole ring. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety. This class does not contain benzimidazole nucleosides and nucleotides.
External Descriptors
Not available