2-Fluoromethcathinone

2-Fluoromethcathinone

Clinical data
Other names	2-FMC; 2-Fluoromethylcathinone; 2-Fluoro-N-methylcathinone; 2-Flephedrone
Drug class	Stimulant; Norepinephrine–dopamine releasing agent
Identifiers
IUPAC name 1-(2-fluorophenyl)-2-(methylamino)propan-1-one
CAS Number	1186137-35-8
PubChem CID	71316821
ChemSpider	37701826
UNII	7NLX9J64KY
CompTox Dashboard (EPA)	DTXSID401017070
Chemical and physical data
Formula	C10H12FNO
Molar mass	181.210 g·mol^−1
3D model (JSmol)	Interactive image
SMILES CC(C(=O)C1=CC=CC=C1F)NC
InChI InChI=1S/C10H12FNO/c1-7(12-2)10(13)8-5-3-4-6-9(8)11/h3-7,12H,1-2H3 Key:DCMOUMKIDLRIBO-UHFFFAOYSA-N

2-Fluoromethcathinone (2-FMC), also known as 2-flephedrone, is a psychostimulant and designer drug of the cathinone family.[1][2][3][4] It acts as a dopamine and norepinephrine releasing agent (NDRA).[4]

Pharmacology

The drug has an EC₅₀Tooltip half-maximal effective concentration for dopamine release of 48.7 nM and induces 85% release of norepinephrine at a concentration of 10 μM.[4] For comparison, the EC₅₀ values of methcathinone are 49.9 nM for dopamine release and 22.4 nM for norepinephrine release and it induces 100% release of norepinephrine at a concentration of 10 μM.[4][5] Hence, compared to methcathinone, 2-FMC appears to be relatively more selective or efficacious for induction of dopamine release over norepinephrine release.[4][5] It is notable in this regard that selective dopamine releasing agents are largely unknown.[6][4]

See also

• 3-Methoxymethcathinone
• 3-Fluoromethcathinone
• 4-Fluoromethcathinone (flephedrone)
• 2-Fluoromethamphetamine

References

1. Kelly JP (2011). "Cathinone derivatives: a review of their chemistry, pharmacology and toxicology". Drug Test Anal. 3 (7–8): 439–453. doi:10.1002/dta.313. PMID 21755607.
2. Glennon RA (2014). "Bath salts, mephedrone, and methylenedioxypyrovalerone as emerging illicit drugs that will need targeted therapeutic intervention". Emerging Targets & Therapeutics in the Treatment of Psychostimulant Abuse. Adv Pharmacol. Vol. 69. pp. 581–620. doi:10.1016/B978-0-12-420118-7.00015-9. ISBN 978-0-12-420118-7. PMC 4471862. PMID 24484988.
3. Kelleher C, Christie R, Lalor K, Fox J, Bowden M, O'Donnell C (30 June 2011). "An Overview of New Psychoactive Substances and the Outlets Supplying them". Reports. doi:10.21427/43F1-XR91. Retrieved 24 November 2024.
4. Blough BE, Decker AM, Landavazo A, Namjoshi OA, Partilla JS, Baumann MH, et al. (March 2019). "The dopamine, serotonin and norepinephrine releasing activities of a series of methcathinone analogs in male rat brain synaptosomes". Psychopharmacology (Berl). 236 (3): 915–924. doi:10.1007/s00213-018-5063-9. PMC 6475490. PMID 30341459.
5. Blough B (July 2008). "Dopamine-releasing agents" (PDF). In Trudell ML, Izenwasser S (eds.). Dopamine Transporters: Chemistry, Biology and Pharmacology. Hoboken [NJ]: Wiley. pp. 305–320. ISBN 978-0-470-11790-3. OCLC 181862653. OL 18589888W.
6. Negus SS, Mello NK, Blough BE, Baumann MH, Rothman RB (February 2007). "Monoamine releasers with varying selectivity for dopamine/norepinephrine versus serotonin release as candidate "agonist" medications for cocaine dependence: studies in assays of cocaine discrimination and cocaine self-administration in rhesus monkeys". J Pharmacol Exp Ther. 320 (2): 627–636. doi:10.1124/jpet.106.107383. PMID 17071819.

External links

• 2-FMC (2-Fluoromethcathinone) - Isomer Design