Methylenedioxycathinone Routes of administration Oral , Insufflation , Rectal ATC code Legal status
(±)-2-amino-1-(3,4-methylenedioxyphenyl)propan-1-one
CAS Number PubChem CID ChemSpider UNII Formula C 10 H 11 N O 3 Molar mass 193.202 g·mol−1 3D model (JSmol )
NC(C(=O)C1=CC2=C(C=C1)OCO2)C
InChI=1S/C10H11NO3/c1-6(11)10(12)7-2-3-8-9(4-7)14-5-13-8/h2-4,6H,5,11H2,1H3
Key:XDEZOLVDJWWXRG-UHFFFAOYSA-N
3,4-Methylenedioxycathinone (also known as MDC , Nitrilone , Amylone and βk-MDA ) is an empathogen and stimulant of the phenethylamine , amphetamine , and cathinone classes[1] [2] and the β-keto analogue of MDA .[3]
Methylenedioxycathinone has been investigated as antidepressant and antiparkinson agent.[4]
See also [ ]
References [ ]
^ Zaitsu K, Katagi M, Tatsuno M, Sato T, Tsuchihashi H, Suzuki K (July 2011). "Recently abused β-keto derivatives of 3,4-methylenedioxyphenylalkylamines: a review of their metabolisms and toxicological analysis". Forensic Toxicology . 29 (2): 73–84. doi :10.1007/s11419-011-0111-8 . S2CID 25416491 .
^ Dal Cason TA, Young R, Glennon RA (December 1997). "Cathinone: an investigation of several N-alkyl and methylenedioxy-substituted analogs". Pharmacology, Biochemistry, and Behavior . 58 (4): 1109–16. doi :10.1016/S0091-3057(97)00323-7 . PMID 9408221 . S2CID 9704972 .
^ Dal Cason TA (May 1997). "The characterization of some 3,4-methylenedioxycathinone (MDCATH) homologs" . Forensic Science International . 87 (1): 9–53. doi :10.1016/S0379-0738(97)02133-6 .
^ WO 1996039133 , Jacob III P, Shulgin AT, "Preparation of novel N-substituted-2-amino-3′,4′-methylenedioxypropiophenones as anti-depressant and anti-parkinsonism agents.", published 12 December 1996, assigned to Neurobiological Technologies, Inc.
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