Structure Information
Structure

Compound Identification

SMILES

CN1C2CCCC1CC(C2)NC(=O)c1[n+](C2OC(C(O)C(O)C2O)C(O)=O)n(C)c2ccccc12

InChIKey

InChIKey=ZITSCJPYYMBLGF-UHFFFAOYSA-O

Formula

C24H33N4O7

Mass

489.548

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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 - Indazole-3-carboxamide - N-glycosyl compound - Glycosyl compound - Indazole - Benzopyrazole - 2-heteroaryl carboxamide - Pyrazole-5-carboxamide - Beta-hydroxy acid - Oxane - Benzenoid - Hydroxy acid - Pyran - Piperidine - Azole - Pyrazole - Heteroaromatic compound - Amino acid - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Azacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organopnictogen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic cation - 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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