Tu banner alternativo

Fencamine

In this article we will delve into the world of Fencamine, exploring its different facets and meanings. Fencamine arouses constant interest in society, whether due to its impact on history, its relevance in the present or its projection into the future. Along these lines, we will dive into a detailed analysis of Fencamine, examining its origins, evolution and possible implications. Whether it is an iconic figure, a cultural phenomenon or a relevant event, Fencamine sparks the interest of specialists and fans alike, providing fertile ground for reflection and debate.

Tu banner alternativo
Fencamine
Clinical data
Trade namesAltimina, Sicoclor
Other namesMethamphetaminoethylcaffeine
Routes of
administration
Oral
Drug classStimulant
ATC code
  • none
Legal status
Legal status
  • In general: ℞ (Prescription only)
Identifiers
  • 1,3,7-trimethyl-8-({2-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 (Altimina, Sicoclor), also known as methamphetaminoethylcaffeine, is a psychostimulant drug of the amphetamine class. It is closely related to fenethylline.[1] It is a prodrug of amphetamine and/or methamphetamine.[2] The drug also contains a caffeine moiety in its chemical structure.

See also

References

  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. ^ 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.