Compound Identification
SMILES
OC[C@@H]1O[C@@H]([C@H](O)[C@H](O)[C@@H]1O)N1N=CC2=CC=CC=C12
InChIKey
InChIKey=BUYAJCVNKKPITI-CLPYTZEMSA-N
Formula
C13H16N2O5
Mass
280.28
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 1-pyranosylindazoles
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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-pyranosylindazoles
Intermediate Tree Nodes
Not available
Direct Parent
1-pyranosylindazoles
Alternative Parents
Glycosylamines Indazoles Oxanes Monosaccharides Benzenoids Pyrazoles Heteroaromatic compounds Secondary alcohols Polyols Oxacyclic compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylindazole - Glycosyl compound - N-glycosyl compound - Benzopyrazole - Indazole - Monosaccharide - Oxane - Benzenoid - Azole - Heteroaromatic compound - Pyrazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-pyranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole 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