Noun:

కునన్ మెడిసిన్,

quinoline's Usage Examples:

It is a structural isomer of quinoline.

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

Although the reaction product is commonly depicted as a quinoline (the enol form), it is believed that the keto form predominates in both the solid state and in solution, making the compound a quinolone.

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

The relative proportions of the hydroxyquinolines (A and B) produced are dependent upon thereaction conditions and structure of the starting material.

VariationsPictet–Spengler tetrahydroisoquinoline synthesisReplacing an indole with a 3,4-dimethoxyphenyl group give the reaction named the Pictet–Spengler tetrahydroisoquinoline synthesis.

acid, glycerol, and an oxidizing agent such as nitrobenzene to yield quinoline.

Some quinoline alkaloids show antiseptic, convulsive or antineoplastic effects.

8-tetra-hydro-4-methoxy-6-methyl-1,3-dioxolos [4,5-g]isoquinolin-5-yl)-1(3H)-isobenzofuranone) and its salts Papaverine (1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxyisoquinoline).

Noscapine (also known as Narcotine, Nectodon, Nospen, Anarcotine and (archaic) Opiane) is a benzylisoquinoline alkaloid, of the phthalideisoquinoline.

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

Berberine is a quaternary ammonium salt from the protoberberine group of benzylisoquinoline alkaloids found in such plants as Berberis, such as Berberis.