Compound Identification
SMILES
CCC1=CC=C(CC2=C3C=CC=CC3=NN2[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1
InChIKey
InChIKey=DDIMTYMXZBVVRO-QMCAAQAGSA-N
Formula
C22H26N2O5
Mass
398.459
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
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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
Hexoses Glycosylamines Indazoles Oxanes Benzene and substituted derivatives Pyrazoles Heteroaromatic compounds Secondary alcohols Polyols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-pyranosylindazole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Benzopyrazole - Indazole - Monocyclic benzene moiety - Benzenoid - Monosaccharide - Oxane - Azole - Heteroaromatic compound - Pyrazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Primary alcohol - Organic oxygen compound - Organonitrogen compound - Organooxygen 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