Аминорекс Википедия
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Аминорекс Википедия
Aminorex Menocil , Apiquel , aminoxaphen , aminoxafen , McN is a weight loss anorectic stimulant drug. It was withdrawn from the market after it was found to cause pulmonary hypertension. Aminorex, in the 2-aminoaryl oxazoline class, was developed by McNeil Laboratories in Aminorex has been shown to have locomotor stimulant effects, lying midway between dextroamphetamine and methamphetamine. Aminorex effects have been attributed to the release of catecholamines. It was discovered in by Edward John Hurlburt , \\\\\\\\\\\\[6\\\\\\\\\\\\] and was quickly found in to have an anorectic effect in rats. It was introduced as a prescription appetite suppressant in Germany , Switzerland and Austria in , but was withdrawn in after it was found to cause pulmonary hypertension in approximately 0. The synthesis was first reported in a structure-activity relationship study of 2-aminoaryloxazolines, where aminorex was found to be approximately 2. From Wikipedia, the free encyclopedia. Aminorex Clinical data ATC code none. IUPAC name. Interactive image. Archived from the original on Jan Analytica Chimica Acta. Journal of Pharmaceutical and Biomedical Analysis. The Journal of Clinical Endocrinology and Metabolism. Potent New Anorectic Agents'. Journal of Medicinal Chemistry. Adapromine Amantadine Bromantane Memantine Rimantadine. Oxiracetam Phenylpiracetam Phenylpiracetam hydrazide. ATC code : N06B. Monoamine releasing agents. Oxazolines: 4-Methylaminorex Aminorex Clominorex Fluminorex. Others: Indeloxazine Viqualine. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy.
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Аминорекс Википедия
Monsta X (RU)
Aminorex Menocil , Apiquel , aminoxaphen , aminoxafen , McN is a weight loss anorectic stimulant drug. It was withdrawn from the market after it was found to cause pulmonary hypertension. Aminorex, in the 2-aminoaryl oxazoline class, was developed by McNeil Laboratories in Aminorex has been shown to have locomotor stimulant effects, lying midway between dextroamphetamine and methamphetamine. Aminorex effects have been attributed to the release of catecholamines. It was discovered in by Edward John Hurlburt , \\\\\\\\\\\\\\[6\\\\\\\\\\\\\\] and was quickly found in to have an anorectic effect in rats. It was introduced as a prescription appetite suppressant in Germany , Switzerland and Austria in , but was withdrawn in after it was found to cause pulmonary hypertension in approximately 0. The synthesis was first reported in a structure-activity relationship study of 2-aminoaryloxazolines, where aminorex was found to be approximately 2. From Wikipedia, the free encyclopedia. Aminorex Clinical data ATC code none. IUPAC name. Interactive image. Archived from the original on Jan Analytica Chimica Acta. Journal of Pharmaceutical and Biomedical Analysis. The Journal of Clinical Endocrinology and Metabolism. Potent New Anorectic Agents'. Journal of Medicinal Chemistry. Adapromine Amantadine Bromantane Memantine Rimantadine. Oxiracetam Phenylpiracetam Phenylpiracetam hydrazide. ATC code : N06B. Monoamine releasing agents. Oxazolines: 4-Methylaminorex Aminorex Clominorex Fluminorex. Others: Indeloxazine Viqualine. Namespaces Article Talk. Views Read Edit View history. In other projects Wikimedia Commons. By using this site, you agree to the Terms of Use and Privacy Policy.
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