Compound Identification
SMILES
OC[C@H]1O[C@H]([C@@H](O)[C@@H](O)[C@@H]1O)N1N=NC2=CC=CC=C12
InChIKey
InChIKey=DGJIWQRFVGEAEV-LDMBFOFVSA-N
Formula
C12H15N3O5
Mass
281.268
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 1-pyranosylbenzotriazoles
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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-pyranosylbenzotriazoles
Intermediate Tree Nodes
Not available
Direct Parent
1-pyranosylbenzotriazoles
Alternative Parents
Hexoses Glycosylamines Benzotriazoles Oxanes Benzenoids Triazoles Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylbenzotriazole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Benzotriazole - Benzenoid - Monosaccharide - Oxane - Azole - Heteroaromatic compound - 1,2,3-triazole - Triazole - 1,2-diol - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Primary alcohol - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-pyranosylbenzotriazoles. These are nucleoside and nucleotide analogs with a structure that consists of a Benzotriazole 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