Compound Identification
SMILES
CO[C@@H]1[C@@H](COCC2=CC=CC=C2)O[C@@H]([C@H](O)[C@H]1OCC1=CC=CC=C1)N1C=CC2=C1C(Cl)=CC=C2
InChIKey
InChIKey=XRCGBLRHZRSHQL-VNOXJOTMSA-N
Formula
C29H30ClNO5
Mass
508.01
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
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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
Glycosylamines N-alkylindoles Benzylethers Indoles Aryl chlorides Substituted pyrroles Oxanes Monosaccharides Heteroaromatic compounds Secondary alcohols Azacyclic compounds Dialkyl ethers Oxacyclic compounds Hydrocarbon derivatives Organochlorides Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-pyranosylindole - Glycosyl compound - N-glycosyl compound - N-alkylindole - Benzylether - Indole or derivatives - Indole - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Monosaccharide - Benzenoid - Substituted pyrrole - Oxane - Heteroaromatic compound - Pyrrole - Secondary alcohol - Oxacycle - Dialkyl ether - Ether - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - 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