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Fencamine

From Wikipedia, the free encyclopedia
Fencamine
Clinical data
Other namesMethamphetaminoethylcaffeine
Routes of
administration
Oral
Drug classStimulant
ATC code
  • none
Identifiers
  • 1,3,7-trimethyl-8-({2-[methyl(1-phenylpropan-2-yl)amino]ethyl}amino)-3,7-dihydro-1H-purine-2,6-dione
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC20H28N6O2
Molar mass384.484 g·mol−1
3D model (JSmol)
  • O=C2N(c1nc(n(c1C(=O)N2C)C)NCCN(C(C)Cc3ccccc3)C)C

Fencamine, also known as methamphetaminoethylcaffeine, is a psychostimulant drug of the amphetamine class. It is closely related to fenethylline.[1] It is metabolized to methamphetamine and amphetamine.[2] The drug also contains a caffeine moiety in its chemical structure.

Fencamine has been experimentally used in the treatment of depression.[2] A clinical report on its use in prolonged reactive depression, an older psychiatric term referring to depressive conditions attributed to psychological stressors, was published in 1970.[3]

A 1974 study described a method for determining fencamine in rat and human urine.[4] According to a 2000 review summarizing the human results, approximately 32% of a 50 mg dose was excreted unchanged in urine within 48 hours.[2]

Names

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The National Center for Advancing Translational Sciences Inxight Drugs database lists Altimina and Sicoclor as names for fencamine hydrochloride.[5]

Yet the United Nations Office on Drugs and Crime's Multilingual Dictionary of Narcotic Drugs and Psychotropic Substances lists these names under fencamfamin.[6]

Sicoclor was a registered medicinal product in Argentina until 2011.[7]

See also

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References

[edit]
  1. ↑ Cody JT (May 2002). "Precursor medications as a source of methamphetamine and/or amphetamine positive drug testing results". Journal of Occupational and Environmental Medicine. 44 (5): 435–50. doi:10.1097/00043764-200205000-00012. PMID 12024689. S2CID 44614179.
  2. 1 2 3 Musshoff F (February 2000). "Illegal or legitimate use? Precursor compounds to amphetamine and methamphetamine". Drug Metab Rev. 32 (1): 15–44. doi:10.1081/dmr-100100562. PMID 10711406.
  3. ↑ Quirós e Isla, P. G. (15 December 1970). "Acción del derivado etilendiamínico, fencamina, sobre depresiones reactivas prolongadas" [Effect of the ethylenediamine derivative, fencamine, on prolonged reactive depression]. Revista Clínica Española (in Spanish). 119 (5): 437–438. PMID 5505078.
  4. ↑ Mallol J, Pitarch L, Coronas R, Pons A Jr (September 1974). "Determination of dl-fencamine in rat and human urine". Arzneimittelforschung. 24 (9): 1301–1304. PMID 4154765.
  5. ↑ "Fencamine hydrochloride". Inxight Drugs. National Center for Advancing Translational Sciences. Retrieved 2026-09-23.
  6. ↑ United Nations Office on Drugs and Crime. "Part One". Multilingual Dictionary of Narcotic Drugs and Psychotropic Substances (PDF). p. 129.
  7. ↑ "Disposición 3520/2011" (PDF) (in Spanish). Administración Nacional de Medicamentos, Alimentos y Tecnología Médica. 17 May 2011. p. 4. Retrieved 25 September 2026.