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Structure Information
Structure

Compound Identification

SMILES

OC1C(O)C(OC(C1O)[n+]1n(cc2cccc(C(O)=N)c12)-c1ccc(cc1)C1CCCNC1)C(O)=O

InChIKey

InChIKey=ZOONJQLGFNIOBC-UHFFFAOYSA-O

Formula

C25H29N4O7

Mass

497.527

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Nucleoside and nucleotide analogues

Subclass

1-pyranosylindazoles

Intermediate Tree Nodes

Not available

Direct Parent

1-pyranosylindazoles

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

1-pyranosylindazole - N-glucuronide - Glucuronic acid or derivatives - Phenylpiperidine - Glycosyl compound - N-glycosyl compound - Phenylpyrazole - Benzopyrazole - Indazole - Beta-hydroxy acid - Aralkylamine - Monocyclic benzene moiety - Hydroxy acid - Oxane - Piperidine - Pyran - Benzenoid - Azole - Pyrazole - Heteroaromatic compound - Amino acid - Secondary alcohol - Amino acid or derivatives - Secondary amine - Secondary aliphatic amine - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Polyol - Carboximidic acid - Carboxylic acid - Carboximidic acid derivative - Carboxylic acid derivative - Oxacycle - Azacycle - Alcohol - Organooxygen compound - Organopnictogen compound - Organic oxide - Amine - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Organic cation - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as 1-pyranosylindazoles. These are nucleoside and nucleotide analogs with a structure that consists of an indazole 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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