Noun:

কুইনাইন্,

quinoline's Usage Examples:

Evoxine (haploperine) is a furoquinoline alkaloid with hypnotic and sedative effects.

It is a structural isomer of quinoline.

Isoquinoline and quinoline are benzopyridines, which are composed of a benzene ring.

3-diazanaphthalene, quinazoline received its name from being an aza derivative of quinoline.

core chemical substructure of the aporphine alkaloids, a subclass of quinoline alkaloids.

\rightleftharpoons } 4,5-dioxo-3a,4,5,6,7,8,9,9b-octahydro-1H-pyrrolo[2,3-f]quinoline- 2,7,9-tricarboxylate + 2 H2O2 + 2 H2O The two substrates of this enzyme.

part of a heterocyclic system, such as imidazole, pyridine, pyrrole, quinoline and thiazole.

, 4-hydroxyquinoline, 4-hydroxyquinoline-3-carboxylic acid, 5,7-CIQA.

As with other quinoline antimalarial drugs, the precise mechanism of action of quinine has not.

reaction of isatin with base and a carbonyl compound to yield substituted quinoline-4-carboxylic acids.

The Knorr quinoline synthesis is an intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using sulfuric acid.

synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives.

The Skraup synthesis is a chemical reaction used to synthesize quinolines.

β-unsaturated carbonyl compounds to form quinolines.

This reaction is also known as the Skraup-Doebner-Von Miller quinoline synthesis, and is named after the.