"changed"@en . . . . "\u041B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D"@ru . . . "Levometorfan, summaformel C18H25NO, \u00E4r en kemisk f\u00F6rening som tillh\u00F6r gruppen opioider. \u00C4mnet kan vara vanebildande och \u00E4r narkotikaklassat. Det anv\u00E4nds inte som l\u00E4kemedel i Sverige. Levometorfan och dextrometorfan \u00E4r optiska isomerer och f\u00F6rekommer i blandad form i racematet racemetorfan. Levometorfan, dextrometorfan och racemetorfan \u00E4r alla narkotikaklassade. Levometorfan och racemetorfan ing\u00E5r i f\u00F6rteckningen N I i 1961 \u00E5rs allm\u00E4nna narkotikakonvention, samt i f\u00F6rteckning II i Sverige, medan dextrometorfan enbart ing\u00E5r i den svenska f\u00F6rteckning V."@sv . "Levometorfan.png"@en . . . . "\u041B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u0301\u043D \u2014 l-\u0441\u0442\u0435\u0440\u0435\u043E\u0438\u0437\u043E\u043C\u0435\u0440 \u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D\u0430. \u042D\u0444\u0444\u0435\u043A\u0442\u044B \u0434\u0432\u0443\u0445 \u0438\u0437\u043E\u043C\u0435\u0440\u043E\u0432 \u043F\u043E\u043B\u043D\u043E\u0441\u0442\u044C\u044E \u0440\u0430\u0437\u043B\u0438\u0447\u043D\u044B. \u0414\u0435\u043A\u0441\u0442\u0440\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u2014 \u043F\u0440\u043E\u0442\u0438\u0432\u043E\u043A\u0430\u0448\u043B\u0435\u0432\u043E\u0435 \u0441\u0440\u0435\u0434\u0441\u0442\u0432\u043E \u0432 \u043D\u0435\u0431\u043E\u043B\u044C\u0448\u0438\u0445 \u0434\u043E\u0437\u0430\u0445 \u0438 \u0434\u0438\u0441\u0441\u043E\u0446\u0438\u0430\u0442\u0438\u0432 \u0432 \u0431\u043E\u043B\u044C\u0448\u0438\u0445, \u0432 \u0442\u043E \u0432\u0440\u0435\u043C\u044F \u043A\u0430\u043A \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u2014 \u043E\u043F\u0438\u043E\u0438\u0434\u043D\u044B\u0439 \u0430\u043D\u0430\u043B\u044C\u0433\u0435\u0442\u0438\u043A. \u042D\u0444\u0444\u0435\u043A\u0442\u044B \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D\u0430 \u0441\u0445\u043E\u0436\u0438 \u0441 \u044D\u0444\u0444\u0435\u043A\u0442\u0430\u043C\u0438 \u043B\u0435\u0432\u043E\u0440\u0444\u0430\u043D\u043E\u043B\u0430, \u043E\u0434\u043D\u0430\u043A\u043E \u043D\u0435\u0441\u043A\u043E\u043B\u044C\u043A\u043E \u0441\u043B\u0430\u0431\u0435\u0435, \u0442\u0430\u043A \u043A\u0430\u043A \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u0434\u043E\u043B\u0436\u0435\u043D \u0444\u0435\u0440\u043C\u0435\u043D\u0442\u0430\u043C\u0438 \u0432 \u043F\u0435\u0447\u0435\u043D\u0438, \u0447\u0442\u043E\u0431\u044B \u0441\u0442\u0430\u0442\u044C \u0430\u043A\u0442\u0438\u0432\u043D\u044B\u043C."@ru . . "S9"@en . . . "Levomethorphan ist ein vollsynthetisch hergestelltes Opioid und der Methylether von Levorphanol. Es geh\u00F6rt zu den nicht verkehrsf\u00E4higen Bet\u00E4ubungsmitteln. Es hat schmerzstillende (analgetische) und hustenstillende Wirkung. Sein Enantiomer Dextromethorphan ist aufgrund der ebenfalls vorhandenen hustenstillenden Wirkung in vielen Hustenblockern (Antitussiva) enthalten, weist hingegen keine schmerzstillenden Eigenschaften auf."@de . . . . . "Lewometorfan \u2013 organiczny zwi\u0105zek chemiczny, eter metylowy leworfanolu, syntetyczny \u015Brodek przeciwb\u00F3lowy dzia\u0142aj\u0105cy agonistycznie na receptory opioidowe (dzia\u0142anie oko\u0142o dwa razy s\u0142absze od morfiny). Przeczytaj ostrze\u017Cenie dotycz\u0105ce informacji medycznych i pokrewnych zamieszczonych w Wikipedii."@pl . . . "None"@en . . "background:#ccccff"@en . . "146176" . . . "COc1ccc2C[C@@H]3[C@@H]4CCCC[C@]4c2c1"@en . . . "5512301"^^ . . . "Class A"@en . "25"^^ . . "6546"^^ . . "Levomethorphan (LVM) (INN, BAN) is an opioid analgesic of the morphinan family that has never been marketed. It is the L-stereoisomer of racemethorphan (methorphan). The effects of the two isomers of the racemethorphan are quite different, with dextromethorphan (DXM) being an antitussive at low doses and a dissociative hallucinogen at much higher doses. Levomethorphan is about five times stronger than morphine. Levomethorphan is a prodrug to levorphanol, analogously to DXM acting as a prodrug to dextrorphan or codeine behaving as a prodrug to morphine. As such, levomethorphan has similar effects to levorphanol but is less potent as it must be demethylated to the active form by liver enzymes before being able to produce its effects. As a prodrug of levorphanol, levomethorphan functions as a potent agonist of all three of the opioid receptors, \u03BC, \u03BA (\u03BA1 and \u03BA3 but notably not \u03BA2), and \u03B4, as an NMDA receptor antagonist, and as a serotonin-norepinephrine reuptake inhibitor. Via activation of the kappa opioid receptor, levomethorphan can produce dysphoria and psychotomimetic effects such as dissociation and hallucinations. Levomethorphan is listed under the Single Convention on Narcotic Drugs 1961 and is regulated like morphine in most countries. In the United States it is a Schedule II Narcotic controlled substance with a DEA ACSCN of 9210 and a 2014 annual aggregate manufacturing quota of 195 grams, up from 6 grams the year before. The salts in use are the tartrate (free base conversion ratio 0.644) and hydrobromide (0.958). At the current time, no levomethorphan pharmaceuticals are marketed in the United States."@en . . . . . . . . . . . . . . . . "\u041B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u0301\u043D \u2014 l-\u0441\u0442\u0435\u0440\u0435\u043E\u0438\u0437\u043E\u043C\u0435\u0440 \u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D\u0430. \u042D\u0444\u0444\u0435\u043A\u0442\u044B \u0434\u0432\u0443\u0445 \u0438\u0437\u043E\u043C\u0435\u0440\u043E\u0432 \u043F\u043E\u043B\u043D\u043E\u0441\u0442\u044C\u044E \u0440\u0430\u0437\u043B\u0438\u0447\u043D\u044B. \u0414\u0435\u043A\u0441\u0442\u0440\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u2014 \u043F\u0440\u043E\u0442\u0438\u0432\u043E\u043A\u0430\u0448\u043B\u0435\u0432\u043E\u0435 \u0441\u0440\u0435\u0434\u0441\u0442\u0432\u043E \u0432 \u043D\u0435\u0431\u043E\u043B\u044C\u0448\u0438\u0445 \u0434\u043E\u0437\u0430\u0445 \u0438 \u0434\u0438\u0441\u0441\u043E\u0446\u0438\u0430\u0442\u0438\u0432 \u0432 \u0431\u043E\u043B\u044C\u0448\u0438\u0445, \u0432 \u0442\u043E \u0432\u0440\u0435\u043C\u044F \u043A\u0430\u043A \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u2014 \u043E\u043F\u0438\u043E\u0438\u0434\u043D\u044B\u0439 \u0430\u043D\u0430\u043B\u044C\u0433\u0435\u0442\u0438\u043A. \u042D\u0444\u0444\u0435\u043A\u0442\u044B \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D\u0430 \u0441\u0445\u043E\u0436\u0438 \u0441 \u044D\u0444\u0444\u0435\u043A\u0442\u0430\u043C\u0438 \u043B\u0435\u0432\u043E\u0440\u0444\u0430\u043D\u043E\u043B\u0430, \u043E\u0434\u043D\u0430\u043A\u043E \u043D\u0435\u0441\u043A\u043E\u043B\u044C\u043A\u043E \u0441\u043B\u0430\u0431\u0435\u0435, \u0442\u0430\u043A \u043A\u0430\u043A \u043B\u0435\u0432\u043E\u043C\u0435\u0442\u043E\u0440\u0444\u0430\u043D \u0434\u043E\u043B\u0436\u0435\u043D \u0444\u0435\u0440\u043C\u0435\u043D\u0442\u0430\u043C\u0438 \u0432 \u043F\u0435\u0447\u0435\u043D\u0438, \u0447\u0442\u043E\u0431\u044B \u0441\u0442\u0430\u0442\u044C \u0430\u043A\u0442\u0438\u0432\u043D\u044B\u043C."@ru . . . . . . . . "462091038"^^ . "Schedule I"@en . "MKXZASYAUGDDCJ-CGTJXYLNSA-N"@en . . . "Levomethorphan"@en . . . . . . . "7"^^ . . . . "5362449" . "Levometorfan, summaformel C18H25NO, \u00E4r en kemisk f\u00F6rening som tillh\u00F6r gruppen opioider. \u00C4mnet kan vara vanebildande och \u00E4r narkotikaklassat. Det anv\u00E4nds inte som l\u00E4kemedel i Sverige. Levometorfan och dextrometorfan \u00E4r optiska isomerer och f\u00F6rekommer i blandad form i racematet racemetorfan. Levometorfan, dextrometorfan och racemetorfan \u00E4r alla narkotikaklassade. Levometorfan och racemetorfan ing\u00E5r i f\u00F6rteckningen N I i 1961 \u00E5rs allm\u00E4nna narkotikakonvention, samt i f\u00F6rteckning II i Sverige, medan dextrometorfan enbart ing\u00E5r i den svenska f\u00F6rteckning V."@sv . . . "-21600.0"^^ . . . . . . . . . . . . . "1908323"^^ . . . . "125"^^ . . . . . . . . . "Levomethorphan"@de . . . . . . "1908323" . . . "Lewometorfan"@pl . . . . . . . "7ZZ22K9QE6" . . . "Levomethorphan (LVM) (INN, BAN) is an opioid analgesic of the morphinan family that has never been marketed. It is the L-stereoisomer of racemethorphan (methorphan). The effects of the two isomers of the racemethorphan are quite different, with dextromethorphan (DXM) being an antitussive at low doses and a dissociative hallucinogen at much higher doses. Levomethorphan is about five times stronger than morphine."@en . . . "-4"^^ . "1"^^ . . . "changed"@en . . "Schedule II"@en . . . . "1112771077"^^ . . . . "1"^^ . "5362449"^^ . . "Levometorfan"@sv . . "Levomethorphan ist ein vollsynthetisch hergestelltes Opioid und der Methylether von Levorphanol. Es geh\u00F6rt zu den nicht verkehrsf\u00E4higen Bet\u00E4ubungsmitteln. Es hat schmerzstillende (analgetische) und hustenstillende Wirkung. Sein Enantiomer Dextromethorphan ist aufgrund der ebenfalls vorhandenen hustenstillenden Wirkung in vielen Hustenblockern (Antitussiva) enthalten, weist hingegen keine schmerzstillenden Eigenschaften auf."@de . "4642423"^^ . . "125-70-2" . . "Lewometorfan \u2013 organiczny zwi\u0105zek chemiczny, eter metylowy leworfanolu, syntetyczny \u015Brodek przeciwb\u00F3lowy dzia\u0142aj\u0105cy agonistycznie na receptory opioidowe (dzia\u0142anie oko\u0142o dwa razy s\u0142absze od morfiny). Przeczytaj ostrze\u017Cenie dotycz\u0105ce informacji medycznych i pokrewnych zamieszczonych w Wikipedii."@pl . . "1"^^ . . . . "18"^^ . . . "146176"^^ . . . "Anlage I"@en .