Compound Identification
SMILES
NC1=CC=CC2=C1N=NN2[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O
InChIKey
InChIKey=XZLZLNNMQHFMLC-AZOIZPIDSA-N
Formula
C12H16N4O5
Mass
296.283
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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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
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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 Polyols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylbenzotriazole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Benzotriazole - Monosaccharide - Oxane - Benzenoid - Heteroaromatic compound - Azole - Triazole - 1,2,3-triazole - Secondary alcohol - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - 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