Structure Information
Structure

Compound Identification

SMILES

CC[C@@H](CO)NCCN[C@@H](CC)CO.COC1=C2N(C=C(C(O)=O)C(=O)C2=CC(F)=C1N1C[C@@H]2CCCN[C@@H]2C1)C1CC1

InChIKey

InChIKey=OWFNFOYLMAYYKF-GYGSSHOESA-N

Formula

C31H48FN5O6

Mass

605.752

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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

Not available

Substituents

Quinoline-3-carboxylic acid - Fluoroquinolone - Dihydroquinolone - Haloquinoline - Aminoquinoline - Dihydroquinoline - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Methoxyaniline - Pyrrolopyridine - Anisole - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - Piperidine - Aryl fluoride - Pyridine - Benzenoid - Aryl halide - Pyrrolidine - Vinylogous amide - Heteroaromatic compound - 1,2-aminoalcohol - Amino acid or derivatives - Amino acid - Tertiary amine - Azacycle - Secondary amine - Carboxylic acid derivative - Carboxylic acid - Secondary aliphatic amine - Ether - Monocarboxylic acid or derivatives - Organopnictogen compound - Amine - Organic oxygen compound - Alcohol - Organic nitrogen compound - Organic oxide - Primary alcohol - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organofluoride - 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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