Structure Information
Structure

Compound Identification

SMILES

OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)N1C=C(CC(=O)N[C@@H](CCC(O)=O)C(O)=O)C2=CC=CC=C12

InChIKey

InChIKey=PPKYVFHFFAMMLR-NDXMBDNFSA-N

Formula

C21H26N2O10

Mass

466.443

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Taxonomic Classification

Taxonomy Tree

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

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-pyranosylindole - Glutamic acid or derivatives - N-acyl-alpha amino acid or derivatives - N-acyl-alpha-amino acid - N-acyl-l-alpha-amino acid - Hexose monosaccharide - Glycosyl compound - N-glycosyl compound - Alpha-amino acid or derivatives - N-alkylindole - 3-alkylindole - Indole or derivatives - Indole - Monosaccharide - Oxane - Dicarboxylic acid or derivatives - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - 1,2-diol - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Organic oxygen compound - Hydrocarbon derivative - Alcohol - Organic nitrogen compound - Carbonyl group - Primary alcohol - Organic oxide - Organooxygen compound - Organonitrogen 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

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