Structure Information
Structure

Compound Identification

SMILES

CN=C(O)c1ccccc1Sc1ccc2c(C=Cc3ccccn3)n(nc2c1)C1OC(C(O)C(O)C1O)C(O)=O

InChIKey

InChIKey=NYVIEWQCOMMMRM-UHFFFAOYSA-N

Formula

C28H26N4O7S

Mass

562.6

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

2-pyranosylindazoles

Intermediate Tree Nodes

Not available

Direct Parent

2-pyranosylindazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

2-pyranosylindazole - N-glucuronide - Glucuronic acid or derivatives - Diarylthioether - N-glycosyl compound - Glycosyl compound - Indazole - Benzopyrazole - Thiophenol ether - Aryl thioether - Beta-hydroxy acid - Monocyclic benzene moiety - Pyridine - Hydroxy acid - Benzenoid - Oxane - Pyran - Azole - Pyrazole - Heteroaromatic compound - Secondary alcohol - Oxacycle - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Sulfenyl compound - Thioether - Polyol - Carbonyl group - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 2-pyranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole base which is N-substituted at the 2-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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