Structure Information
Structure

Compound Identification

SMILES

[H]OC(=O)C([H])([H])C1=C([H])N(C2=C([H])C([H])=C([H])C([H])=C12)[C@@]1([H])O[C@]([H])(C([H])([H])O[H])[C@]([H])(O[H])[C@]([H])(O[H])[C@@]1([H])O[H]

InChIKey

InChIKey=MVSQEPAOMLRIRW-CHUNWDLHSA-N

Formula

C16H19NO7

Mass

337.328

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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 - Indolyl carboxylic acid derivative - N-glycosyl compound - Glycosyl compound - N-alkylindole - Indole or derivatives - Indole - Hydroxy fatty acid - Heterocyclic fatty acid - Branched fatty acid - Fatty acyl - Benzenoid - Substituted pyrrole - Oxane - Heteroaromatic compound - Pyrroline - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen 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

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