Compound Identification
SMILES
OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)N1C(=O)NC2=CC=CC=C12
InChIKey
InChIKey=CWOLCJVCLXGDPO-RMPHRYRLSA-N
Formula
C13H16N2O6
Mass
296.279
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 1-pyranosylbenzimidazoles
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
1-pyranosylbenzimidazoles
Intermediate Tree Nodes
Not available
Direct Parent
1-pyranosylbenzimidazoles
Alternative Parents
Hexoses Glycosylamines Benzimidazoles Benzenoids N-substituted imidazoles Oxanes Heteroaromatic compounds Secondary alcohols Ureas 1,2-diols Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Primary alcohols Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylbenzimidazole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Benzimidazole - Benzenoid - Monosaccharide - N-substituted imidazole - Oxane - Azole - Heteroaromatic compound - Imidazole - 1,2-diol - Urea - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Primary alcohol - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-pyranosylbenzimidazoles. These are nucleoside and nucleotide analogs with a structure that consists of a Benzimidazole which is N-substituted at the 1-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
External Descriptors
Not available