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Structure Information
Structure

Compound Identification

SMILES

CSC(SC)=NC(=O)C1=CN(C2OC(CO)C(O)C2O)C2=CC=CC=C12

InChIKey

InChIKey=CDZQYXMQVUVHDW-UHFFFAOYSA-N

Formula

C17H20N2O5S2

Mass

396.48

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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

1-ribofuranosylindole - Indolecarboxamide derivative - Indolecarboxylic acid derivative - Glycosyl compound - N-glycosyl compound - N-alkylindole - Pentose monosaccharide - Indole - Indole or derivatives - Pyrrole-3-carboxamide - Pyrrole-3-carboxylic acid or derivatives - Benzenoid - Substituted pyrrole - Monosaccharide - Pyrrole - Vinylogous amide - Oxolane - Heteroaromatic compound - Secondary alcohol - 1,2-diol - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Oxacycle - Alcohol - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organosulfur compound - 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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