Open Access Articles- Top Results for 2-Fluoroamphetamine


Ball-and-stick model of the 2-fluoroamphetamine molecule
Systematic (IUPAC) name
Clinical data
1716-60-5 7pxN
PubChem CID 121531
ChemSpider 108441 7pxY
Chemical data
Formula C9H12FN
153.196 g/mol
 14pxN (what is this?)  (verify)
1 gram of 2-FA

2-Fluoroamphetamine (2-FA) is a stimulant drug from the amphetamine family which has been sold as a designer drug.[1] 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 the substitute.[2][3]


Anorexiant dose (amount inhibiting food intake by 50% for 2 hours, given 1 hour earlier) = 15 mg/kg (rat; p.o.).[4]

Analgesic dose (50% inhibition of response to tail-clamp) = 20 mg/kg (mouse; i.p.).[4]

Effect on blood pressure: 0.5 mg/kg (rat; i.v.) produces an increase in BP of 29 mm.[4]


LD50 (mouse; i.p.) = 100 mg/kg.[4]

See also


  1. ^ Rösner, P; Quednow, B; Girreser, U; Junge, T (2005). "Isomeric fluoro-methoxy-phenylalkylamines: a new series of controlled-substance analogues (designer drugs)". Forensic Science International 148 (2–3): 143–56. PMID 15639609. doi:10.1016/j.forsciint.2004.05.003. 
  2. ^ B.E. Smart (2001). "Fluorine substituent effects (on bioactivity". Journal of Fluorine Chemistry 109: 3–11. doi:10.1016/s0022-1139(01)00375-x. 
  3. ^ F.M.D. Ismail (2002). "Important fluorinated drugs in experimental and clinical use". Journal of Fluorine Chemistry 118: 27–33. doi:10.1016/s0022-1139(02)00201-4. 
  4. ^ a b c d E. Costa and S. Garattini (1970) Amphetamines and Related Compounds, p.28, New York: Raven Press.

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