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*  Hemozoin
Sullivan DJ (December 2002). "Theories on malarial pigment formation and quinoline action". Int J Parasitol. 32 (13): 1645-53. ... The best-understood examples of such hematin biocrystallization inhibitors are quinoline drugs such as chloroquine and ... "Interference with Hemozoin Formation Represents an Important Mechanism of Schistosomicidal Action of Antimalarial Quinoline ...
*  Quinoline
... is only slightly soluble in cold water but dissolves readily in hot water and most organic solvents. Quinoline itself ... Quinoline was first extracted from coal tar in 1834 by German chemist Friedlieb Ferdinand Runge; he called quinoline leukol (" ... "Quinoline". Encyclopædia Britannica. 1911. Gerd Collin; Hartmut Höke (2005), "Quinoline and Isoquinoline", Ullmann's ... Quinolines are present in small amounts in crude oil within the virgin diesel fraction. It can be removed by the process called ...
*  Quinoline Yellow
... may refer to: Either of two chemically related dyes: Quinoline Yellow SS, a bright yellow dye Quinoline Yellow ...
*  Combes quinoline synthesis
There are multiple ways to synthesize quinoline, one of which is the Combes quinoline synthesis. The synthesis of quinoline ... The Combes quinoline synthesis is often used to prepare the 2,4-substituted quinoline backbone and is unique in that it uses a ... resulting in the end product of a substituted quinoline. The formation of the quinoline product is influenced by the ... "Quinolines". Sigma-Aldrich. Sigma-Aldrich Co. LLC. Retrieved 7 December 2013. Luo, Z.G.; Zeng, C.C; Wang, F.; HE, H.Q.; Wang, C ...
*  Niementowski quinoline synthesis
The Niementowski quinoline synthesis is the chemical reaction of anthranilic acids and ketones (or aldehydes) to form γ- ... There is then a loss of water that leads to a ring closing and formation of the quinoline derivative. Most evidence supports ... Wang, M. -X., Liu, Y., Huang, Z, -T.; Liu; Huang (2001). "Novel and convenient synthesis of polyfunctionalized quinolines, ... 376-384 Manske, R. H. (1942). "The Chemistry of Quinolines". Chem. Rev. 30: 127. doi:10.1021/cr60095a006. Hisano, T. (1973). " ...
*  Quinoline Yellow SS
Quinoline yellow is representative of a large class of quinophthalone pigments. It is suggested that quinoline yellow exhibits ... When sulfonated, it converts to a water-soluble derivative, Quinoline Yellow WS. Quinoline Yellow SS is used in spirit lacquers ... Quinoline Yellow SS is a bright yellow dye with green shade. It is insoluble in water, but soluble in nonpolar organic solvents ... Quinoline Yellow SS is used in some yellow colored smoke formulations. It may cause contact dermatitis. It has the appearance ...
*  Quinoline Yellow WS
... is a mixture of organic compounds derived from the dye Quinoline Yellow SS (Spirit Soluble). Owing to the ... Quinoline Yellow WS has not been associated with any significant long-term toxicity, is not genotoxic or carcinogenic and there ... In the EU and Australia, Quinoline Yellow is permitted in beverages and is used in foods, like sauces, decorations, and ... freepatentsonline.com - Process for purification of quinoline yellow efsa.europa.eu - EFSA updates safety advice on six food ...
*  Quinoline 2-oxidoreductase
In enzymology, a quinoline 2-oxidoreductase (EC 1.3.99.17) is an enzyme that catalyzes the chemical reaction quinoline + ... Bauder R, Tshisuaka B, Lingens F (1990). "Microbial metabolism of quinoline and related compounds. VII Quinoline oxidoreductase ... XII Isolation and characterization of the quinoline oxidoreductase from Rhodococcus spec. B1 compared with the quinoline ... The systematic name of this enzyme class is quinoline:acceptor 2-oxidoreductase (hydroxylating). As of late 2007, only one ...
*  Knorr quinoline synthesis
The Knorr quinoline synthesis is an intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using ...
*  Camps quinoline synthesis
The Camps quinoline synthesis (also known as the Camps cyclization) is a chemical reaction whereby an o-acylaminoacetophenone ... Although the reaction product is commonly depicted as a quinoline (the enol form), it is believed that the keto form ...
*  Quinoline-4-carboxylate 2-oxidoreductase
"Microbial metabolism of quinoline and related compounds. XV Quinoline-4-carboxylic acid oxidoreductase from Agrobacterium spec. ... In enzymology, a quinoline-4-carboxylate 2-oxidoreductase (EC 1.3.99.19) is an enzyme that catalyzes the chemical reaction ... The systematic name of this enzyme class is quinoline-4-carboxylate:acceptor 2-oxidoreductase (hydroxylating). Other names in ... reduced acceptor The 3 substrates of this enzyme are quinoline-4-carboxylate, acceptor, and H2O, whereas its two products are 2 ...
*  Skraup reaction
The Skraup synthesis is a chemical reaction used to synthesize quinolines. It is named after the Czech chemist Zdenko Hans ... Manske, R. H. F. (1942). "The Chemistry of Quinolines". Chem. Rev. 30: 113. doi:10.1021/cr60095a006. Manske, Richard H. F.; ... doi:10.1016/S0040-4020(01)98495-9. Clarke, H. T.; Davis, A. W. (1941). "Quinoline". Org. Synth. CS1 maint: Multiple names: ... and an oxidizing agent such as nitrobenzene to yield quinoline. In this example, nitrobenzene serves as both the solvent and ...
*  Friedländer synthesis
Jia, C.-S.; Zhang, Z.; Tu, S.-J.; Wang, G.-W. (2006). "Rapid and efficient synthesis of poly-substituted quinolines assisted by ... Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline". Chem. Rev. 35 (2): 77-277. doi:10.1021/cr60111a001. Cheng, C.-C ... Wu, J.; Xia, H.-G.; Gao, K. (2006). "Molecular iodine: A highly efficient catalyst in the synthesis of quinolines via ... The Friedländer synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives. It is ...
*  Pfitzinger reaction
Reaction of N-acyl isatins with base gives 2-hydroxy-quinoline-4-carboxylic acids. Camps quinoline synthesis Friedländer ... Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline". Chem. Rev. 35 (2): 77-277. doi:10.1021/cr60111a001. Shvekhgeimer ... Manske, R. H. (1942). "The Chemistry of Quinolines". Chem. Rev. 30 (1): 113-144. doi:10.1021/cr60095a006. Bergstrom, F. W. ( ... is the chemical reaction of isatin with base and a carbonyl compound to yield substituted quinoline-4-carboxylic acids. Several ...
*  Lepidine
Quinaldine, the isomer with the methyl group in position 2. Quinoline. ...
*  Pyridinium perbromide
The analogous quinoline compound behaves similarly. Pyridinium tribromide can be obtained by reacting pyridinium hydrobromide ... The Chemistry of Heterocyclic Compounds, Quinolines. Wiley. p. 615. Houben-Weyl Methods of Organic Chemistry (in German). 4: ...
*  Discovery and development of TRPV1 antagonists
8-quinoline > 8-quinazoline > 8-isoquinoline ≥ cinnoline > phthalazine > quinoxaline > 5-quinoline e.g. AMG517 (fig. 8b), ... structure-activity relationships for ureas with quinoline, isoquinoline, quinazoline, phthalazine, quinoxaline, and cinnoline ...
*  Nitroquinoline-N-oxide reductase
The systematic name of this enzyme class is 4-(hydroxyamino)quinoline N-oxide:NADP+ oxidoreductase. Other names in common use ... Toriyama N (1965). "[Metabolism of quinoline derivatives. On the reducing enzyme of 4-nitroquinoline-N-oxide]". Nichidai Igaku ... quinoline N-oxide + 2 NAD(P)+ + H2O ⇌ {\displaystyle \rightleftharpoons } 4-nitroquinoline N-oxide + 2 NAD(P)H + 2 H+ The 4 ...
*  Quinaldine
It is one of the methyl derivative of a heterocyclic compound quinoline. It is bioactive and is used in the preparation of ... Quinaldine is used in anti-malaria drugs, in manufacturing dyes, food colorants (e.g., Quinoline Yellows, pinacyanol), ... Gerd Collin; Hartmut Höke (2005), "Quinoline and Isoquinoline", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley ...
*  Paul K. Calaway
"Graduate Chemist Develops Three New Quinoline Drugs". The Technique. 1942-02-20. Retrieved 2010-02-02. "A study of quinoline ...
*  Asymmetric hydrogenation
Wang, Z. J.; Deng, G. J.; Li, Y.; He, Y. M.; Tang, W. J.; Fan, Q. H. (2007). "Enantioselective Hydrogenation of Quinolines ... Two systems exist for the asymmetric hydrogenation of 2-substituted quinolines with isolated yields generally greater than 80% ... Reetz, M. T.; Li, X. (2006). "Asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived ... Quinolines". Journal of the American Chemical Society. 125 (35): 10536-10537. doi:10.1021/ja0353762. PMID 12940733. Xu, L.; Lam ...
*  Conrad-Limpach synthesis
showed that many quinoline derivatives show promise in their anti-inflammatory effects for the treatment of arthritis,[6] ... With much of the literature on the synthesis of quinolines, there is some discrepancy on whether a substituted 4- ... The majority of drugs in clinical use are actually quinoline derivatives that belong to the subset fluoroquinolones, which have ... studied the use of quinoline derivatives as HIV-1 integrase inhibitors.[8] Conrad, M.; Limpach, L. synthesen von ...
*  Acridine
Like the related molecule pyridine and quinoline, acridine is mildly basic. It is an almost colorless solid. There are no ... It also shares properties with quinoline. Acridines can be reduced to the 9,10-dihydroacridines, sometimes called leuco ... On oxidation with potassium permanganate, it yields acridinic acid (C9H5N(CO2H)2) otherwise known as quinoline-1,2-dicarboxylic ...
*  Food coloring
Quinoline Yellow WS, which is yellow. Food portal Azo compound Acid dye E number Federal Food, Drug, and Cosmetic Act Food ... In Germany, for example, quinoline yellow was allowed in puddings and desserts, but tartrazine was not. The reverse was true in ... March 2011 [Guidelines on approaches to the replacement of Tartrazine, Allura Red, Ponceau 4R, Quinoline Yellow, Sunset Yellow ... Quinoline Yellow E122: Carmoisine E124: Ponceau 4R E131: Patent Blue V E142: Green S In the US, the following seven artificial ...
*  Doebner-Miller reaction
Combes quinoline synthesis Doebner reaction Gould-Jacobs reaction Knorr quinoline synthesis Skraup synthesis Doebner, O.; ... This reaction is also known as the Skraup-Doebner-Von Miller quinoline synthesis, and is named after the Czech chemist Zdenko ... The Doebner-Miller reaction is the organic reaction of an aniline with α,β-unsaturated carbonyl compounds to form quinolines. ... Hexacyclic Compounds: Pyridine, Quinoline, and Isoquinoline". Chem. Rev. 35 (2): 153. doi:10.1021/cr60111a001. Denmark, Scott E ...