Exploring Selegiline. To explore a different substance…

IUPAC name:
2443 · C13H17N · 187.281
MEZLKOACVSPNER-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Scorza, M; Carrau, C; Silveira, R; Zapata-Torres, G; Cassels, BK; Reyes-Parada, M. Monoamine oxidase inhibitory properties of some methoxylated and alkylthio amphetamine derivatives. Biochem. Pharmacol., 15 Dec 1997, 54 (12), 1361–1369. 697 kB. https://doi.org/10.1016/S0006-2952(97)00405-X #2

Shulgin, AT. Peyote and MAO inhibitors. Ask Dr. Shulgin Online, Center for Cognitive Liberty & Ethics, 14 Nov 2001.

Magyar, K. The pharmacology of selegiline. Int. Rev. Neurobiol., 2011, 100, 65–84. 168 kB. https://doi.org/10.1016/B978-0-12-386467-3.00004-2

Thunhorst, M; Holzgrabe, U. Utilizing NMR spectroscopy for assessing drug enantiomeric composition. Magn. Reson. Chem., 1 Mar 1998, 36 (3), 211–216. 237 kB. https://doi.org/10.1002/(SICI)1097-458X(199803)36:3<211::AID-OMR246>3.0.CO;2-Y

Nakanishi, K; Miki, A; Zaitsu, K; Kamata, H; Shima, N; Kamata, T; Katagi, M; Tatsuno, M; Tsuchihashi, H; Suzuki, K. Cross-reactivities of various phenethylamine-type designer drugs to immunoassays for amphetamines, with special attention to the evaluation of the one-step urine drug test Instant-View™, and the Emit® assays for use in drug enforcement. Forensic Sci. Int., 10 Apr 2012, 217 (1–3), 174–181. 397 kB. https://doi.org/10.1016/j.forsciint.2011.11.003

Musshoff, F. Illegal or legitimate use? Precursor compounds to amphetamine and methamphetamine. Drug Metab. Rev., 2000, 32 (1), 15–44. 376 kB. https://doi.org/10.1081/DMR-100100562

Wagmann, L; Brandt, SD; Kavanagh, PV; Maurer, HH; Meyer, MR. In vitro monoamine oxidase inhibition potential of alpha-methyltryptamine analog new psychoactive substances for assessing possible toxic risks. Toxicol. Lett., 17 Apr 2017, 272, 84–93. 1.9 MB. https://doi.org/10.1016/j.toxlet.2017.03.007

(Phenanthrenamine) PCA
19 June 2018 · Creative Commons BY-NC-SA ·