Compound Identification
SMILES
OC[C@H]1O[C@@H]([C@H](O)[C@@H](O)[C@H]1O)N1C=C2C=CC=CC2=N1
InChIKey
InChIKey=TVMIXKONFVVSSC-SJHCENCUSA-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 2-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
2-pyranosylindazoles
Intermediate Tree Nodes
Not available
Direct Parent
2-pyranosylindazoles
Alternative Parents
Glycosylamines Indazoles Oxanes Monosaccharides Benzenoids Pyrazoles Heteroaromatic compounds Secondary alcohols 1,2-diols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-pyranosylindazole - Glycosyl compound - N-glycosyl compound - Benzopyrazole - Indazole - Benzenoid - Monosaccharide - Oxane - Azole - Heteroaromatic compound - Pyrazole - 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 2-pyranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole base which is N-substituted at the 2-position with a pyranose moiety. Nucleotide analogues contain a phosphate group linked to the C5 carbon atom of the pyranose.
External Descriptors
Not available