Compound Identification
SMILES
NC1=C(N=CN1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O)C1=C(Br)C=NN1
InChIKey
InChIKey=XAWHFLAKBYKTCP-MGUDNFKCSA-N
Formula
C11H14BrN5O4
Mass
360.168
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 Aminoimidazoles Aryl bromides N-substituted imidazoles Pyrazoles Oxolanes Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organobromides Primary alcohols Primary amines
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Imidazole ribonucleoside - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - Aminoimidazole - Aryl bromide - Aryl halide - Monosaccharide - N-substituted imidazole - Azole - Heteroaromatic compound - Imidazole - Oxolane - Pyrazole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Primary amine - Amine - Organohalogen compound - Organobromide - Alcohol - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Primary alcohol - 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