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quinoline

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quinoline
quinoline Chem. (ˈkwɪnəlaɪn) Also -olein(e. [f. as prec. + -ine5.] = chinoline.1845 W. Gregory Outl. Org. Chem. 481 Quinoline..is formed artificially, by distilling quinine, cinchonine, or strychnine, along with caustic potash. 1845 Penny Cycl. Suppl. I. 350/1 The taste of quinolein is very acrid an... Oxford English Dictionary
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Quinoline
Occurrence and isolation Quinoline was first extracted from coal tar in 1834 by German chemist Friedlieb Ferdinand Runge; he called quinoline leukol ( Coal tar remains the principal source of commercial quinoline. wikipedia.org
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Investigating biological activity spectrum for novel quinoline ...
Investigating biological activity spectrum for novel quinoline analogues. by Robert Musiol, Josef Jampilek, Katarina Kralova, Des R Richardson, Danuta Kalinowski, Barbara Podeszwa, Jacek Finster, Halina Niedbala, Anna Palka, Jaroslaw Polanski. Bioorganic & medicinal chemistry. Read more related scholarly scientific articles and abstracts.
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Quinoline Yellow
Quinoline Yellow may refer to two chemically related dyes: Quinoline Yellow SS, a bright yellow dye Quinoline Yellow WS, a yellow food coloring It may wikipedia.org
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Quinoline Yellow SS
Quinoline yellow is representative of a large class of quinophthalone pigments. References Quinoline dyes Staining dyes Solvent dyes Indandiones wikipedia.org
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Quinoline methiodide
Quinoline methiodide is a quaternary ammonium compound produced by reaction of quinoline with methyl iodide. It has paralyzing effects. wikipedia.org
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Quinoline Yellow WS
Quinoline Yellow WS is a mixture of organic compounds derived from the dye Quinoline Yellow SS (spirit soluble). In the EU and Australia, Quinoline Yellow is permitted in beverages and is used in foods, like sauces, decorations, and coatings; Quinoline Yellow is wikipedia.org
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Quinoline 2-oxidoreductase
In enzymology, a quinoline 2-oxidoreductase () is an enzyme that catalyzes the chemical reaction quinoline + acceptor + H2O quinolin-1(2H)-one + reduced The systematic name of this enzyme class is quinoline:acceptor 2-oxidoreductase (hydroxylating). wikipedia.org
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WO2020233723A1 - Quinoline derivatives for treatment of head and neck ...
Provided is an application of a compound, 1-[[[4-(4-fluoro-2-methyl-1H-indol-5-yl)oxy-6-methoxyquinolin-7-yl]oxy]methyl]cyclopropylamine, in preparation of a medicament for the treatment of head and neck cancer, and an application of a pharmaceutical composition of the compound combined with a second therapeutic drug in the preparation of a medicament for the treatment of head and neck cancer.
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Quinoline alkaloids
Quinoline alkaloids are naturally occurring chemical compounds from the group of alkaloids, which are chemically derived from quinoline. Strychnine and brucine, alkaloids of the nux vomica, which have a hydrogenated quinoline system, are also counted among the quinoline alkaloids. wikipedia.org
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WO2020228656A1 - Quinoline derivative used for soft tissue sarcoma ...
A quinoline derivative used for soft tissue sarcoma combination therapy, relating to a use of the quinoline derivative in combination with a second therapeutic drug to treat soft tissue sarcoma, wherein the second therapeutic drug may be a chemotherapy drug, a small molecule targeted anti-tumour drug or an immunotherapy drug. The chemical name of the quinoline derivative compound I is 1-[[[4 ...
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Niementowski quinoline synthesis
There is then a loss of water that leads to a ring closing and formation of the quinoline derivative. See also Camps quinoline synthesis Friedländer synthesis Pfitzinger reaction Condensation reactions Quinoline forming reactions Name reactions wikipedia.org
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Combes quinoline synthesis
The Combes quinoline synthesis is often used to prepare the 2,4-substituted quinoline backbone and is unique in that it uses a β-diketone substrate, which Importance of Quinoline Synthesis There are multiple ways to synthesize quinoline, one of which is the Combes quinoline synthesis. wikipedia.org
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Camps quinoline synthesis
The Camps quinoline synthesis (also known as the Camps cyclization) is a chemical reaction whereby an o-acylaminoacetophenone is transformed into two different References See also Conrad-Limpach synthesis Doebner reaction Quinoline forming reactions Name reactions wikipedia.org
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Knorr quinoline synthesis
The Knorr quinoline synthesis is an intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using sulfuric acid. For preparative purposes triflic acid is recommended: References Quinoline forming reactions Name reactions wikipedia.org
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