Structure Information
Structure

Compound Identification

SMILES

CC1CCCN(C1)C1=C(F)C=C2C(=O)C(=CN(C3=CN(C)C=C3[N+]([O-])=O)C2=C1)C(O)=O

InChIKey

InChIKey=MPYZQAMQBYHHOH-UHFFFAOYSA-N

Formula

C21H21FN4O5

Mass

428.42

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Quinolines and derivatives

Subclass

Quinoline carboxylic acids

Intermediate Tree Nodes

Not available

Direct Parent

Quinoline carboxylic acids

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Quinoline-3-carboxylic acid - Fluoroquinolone - Aminoquinoline - Haloquinoline - Dihydroquinolone - Dihydroquinoline - Pyridine carboxylic acid or derivatives - Pyridine carboxylic acid - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Piperidine - N-methylpyrrole - Pyridine - Aryl halide - Substituted pyrrole - Benzenoid - Aryl fluoride - Heteroaromatic compound - Vinylogous amide - Pyrrole - Tertiary amine - Amino acid - C-nitro compound - Organic nitro compound - Amino acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Carboxylic acid - Organic oxoazanium - Azacycle - Allyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Organohalogen compound - Amine - Hydrocarbon derivative - Organic zwitterion - Organofluoride - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic salt - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.

External Descriptors

Not available

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