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Fluoroamphetamine
Fluoroamphetamine may refer to: * 2-Fluoroamphetamine * 3-Fluoroamphetamine * 4-Fluoroamphetamine 4-Fluoroamphetamine (4-FA; 4-FMP; PAL-303; "Flux"), also known as ''para''-fluoroamphetamine (PFA) is a psychoactive research chemical of the phenethylamine and substituted amphetamine chemical classes. It produces stimulant and entactogenic ef ... {{Short pages monitor ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
3-Fluoroamphetamine
3-Fluoroamphetamine (3-FA; PAL-353) is a stimulant drug from the amphetamine family which acts as a monoamine releaser with similar potency to methamphetamine but more selectivity for dopamine and norepinephrine release over serotonin. It is self-administered by mice to a similar extent to related drugs such as 4-fluoroamphetamine and 3-methylamphetamine. Legal status China As of October 2015 3-FA is a controlled substance in China. See also * 2-Fluoroamphetamine (2-FA) * 3-Fluoroethamphetamine 3-Fluoroethamphetamine (3-FEA) is a stimulant drug of the amphetamine class which acts as a releasing agent of the monoamine neurotransmitters norepinephrine, dopamine and serotonin. Compared to the unsubstituted ethylamphetamine, 3-fluoroetha ... (3-FEA) * 3-Fluoromethamphetamine (3-FMA) * 3-Hydroxyamphetamine (Gepefrine) * 3-Methylamphetamine (3-MA) * 3-Methoxyamphetamine (3-MeOA) * 3-Trifluoromethylamphetamine (Norfenfluramine) * 4-Fluoroamphetamine (4-FA) References ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
2-Fluoroamphetamine
2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug. 2-Fluoroamphetamine differs from 3- and 4-fluoroamphetamine in the position of the fluorine atom on the aromatic ring, making them positional isomers of one another. The replacement of a hydrogen atom with a fluorine atom in certain compounds to facilitate passage through the blood–brain barrier, as is desirable in central nervous system pharmaceutical agents, is a common practice due to the corresponding increase in lipophilicity granted by this substitution. Pharmacology Anorexiant dose (amount inhibiting food intake by 50% for 2 hours, given 1 hour earlier) = 15 mg/kg (rat; p.o.). Analgesic dose (50% inhibition of response to tail-clamp) = 20 mg/kg (mouse; i.p.). Effect on blood pressure: 0.5 mg/kg (rat; i.v.) produces an increase in BP of 29 mm. Toxicology LD50 (mouse; i.p.) = 100 mg/kg. Legal Status United States The Federal ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
