Compound Identification
SMILES
CC(=O)C1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=CC=CC=C12
InChIKey
InChIKey=MECZJOZYNBFIDH-IBEHDNSVSA-N
Formula
C16H19NO6
Mass
321.329
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
- Subclass 1-pyranosylindoles
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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-pyranosylindoles
Intermediate Tree Nodes
Not available
Direct Parent
1-pyranosylindoles
Alternative Parents
Hexoses Glycosylamines N-alkylindoles Indoles Aryl alkyl ketones Oxanes Substituted pyrroles Benzenoids Heteroaromatic compounds Vinylogous amides 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary alcohols Organonitrogen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylindole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - N-alkylindole - Indole - Indole or derivatives - Aryl alkyl ketone - Aryl ketone - Monosaccharide - Oxane - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Vinylogous amide - Pyrrole - 1,2-diol - Ketone - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Polyol - Organooxygen compound - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-pyranosylindoles. These are nucleoside and nucleotide analogs with a structure that consists of an indole base 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