Compound Identification
SMILES
CC(C)(O)C(O)CC1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C2=CC=CC=C12
InChIKey
InChIKey=NJNIHOLHKRAEFY-YEUAOBPJSA-N
Formula
C19H27NO7
Mass
381.425
Taxonomic Classification
Taxonomy Tree
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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
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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 3-alkylindoles N-alkylindoles Oxanes Substituted pyrroles Benzenoids Heteroaromatic compounds Tertiary alcohols 1,2-diols Secondary alcohols Oxacyclic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives Primary alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylindole - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - N-alkylindole - 3-alkylindole - Indole - Indole or derivatives - Monosaccharide - Oxane - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Tertiary alcohol - 1,2-diol - Secondary alcohol - Polyol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - 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