Structure Information
Structure

Compound Identification

SMILES

CN1C[C@H](CO)C[C@H]2[C@H]1CC1=CN([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)C3=CC=CC2=C13

InChIKey

InChIKey=PQVPZDKAHKYFBK-HCSLTRCHSA-N

Formula

C21H28N2O5

Mass

388.464

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Indole ribonucleosides and ribonucleotides

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Indole ribonucleosides and ribonucleotides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Clavine skeleton - 1-ribofuranosylindole - Ergoline skeleton - Indoloquinoline - Benzoquinoline - Pyrroloquinoline - Glycosyl compound - N-glycosyl compound - Pentose monosaccharide - 3-alkylindole - Quinoline - N-alkylindole - Indole or derivatives - Isoindole or derivatives - Alkaloid or derivatives - Indole - Aralkylamine - Benzenoid - Piperidine - Substituted pyrrole - Monosaccharide - 1,3-aminoalcohol - Heteroaromatic compound - Oxolane - Pyrrole - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Alcohol - Hydrocarbon derivative - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Amine - Primary alcohol - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as indole ribonucleosides and ribonucleotides. These are compounds in which the C-1 of a ribosyl (or deoxyribosyl) moiety is linked to the N1-position of an indole. Nucleotides have a phosphate group linked to the C5 carbon of the ribose (or deoxyribose) moiety.

External Descriptors

Not available

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