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Substituted cathinone

Substituted cathinones, or simply cathinones, which include some stimulants and entactogens, are derivatives of cathinone. They feature a phenethylamine core with an alkyl group attached to the alpha carbon, and a ketone group attached to the beta carbon, along with additional substitutions.[1][2][3][4][5] Cathinone occurs naturally in the plant khat whose leaves are chewed as a recreational drug.[6]

Cathinone
General chemical structure of substituted cathinones, with R1-R4 defined in text

Substituted cathinones act as monoamine releasing agents and/or monoamine reuptake inhibitors, including of norepinephrine, dopamine, and/or serotonin.[7][8][9][10][11][12] In contrast to substituted amphetamines, substituted cathinones do not act as agonists of the human trace amine-associated receptor 1 (TAAR1).[13][14][15] This may potentiate their stimulating and addictive effects.[13][14]

List of substituted cathinones

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The derivatives may be produced by substitutions at four locations of the cathinone molecule:

  • R1 = hydrogen, or any combination of one or more alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents
  • R2 = hydrogen or any alkyl group
  • R3 = hydrogen, any alkyl group, or incorporation in a cyclic structure
  • R4 = hydrogen, any alkyl group, or incorporation in a cyclic structure

The following table displays notable derivatives that have been reported:[16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37]


Structure Compound R1 R2 R3 R4 CAS number
  Cathinone H Me H H 71031-15-7
  Methcathinone H Me H Me 5650-44-2
  Ethcathinone H Me H Et 51553-17-4
  Propylcathinone H Me H nPr 52597-14-5
  Buphedrone H Et H Me 408332-79-6
  N-Ethylbuphedrone (NEB) H Et H Et 1354631-28-9
  N-Methyl-N-ethylbuphedrone H Et Me Et
  Pentedrone H nPr H Me 879722-57-3
  N-Ethylpentedrone H nPr H Et 18268-16-1
  N-Isopropylpentedrone H nPr H iPr 18268-14-9
  Hexedrone H nBu H Me 2169446-41-5
  N-Ethylhexedrone H nBu H Et 18410-62-3
  N-Butylhexedrone H nBu H nBu 18296-66-7
  N-Isobutylhexedrone (NDH) H nBu H i-Bu
  Isohexedrone H iBu H Me
  N-Ethylheptedrone H nPe H Et
  Octedrone H hexyl H Me
  Dimethylcathinone H Me Me Me 15351-09-4
  Diethylpropion H Me Et Et 134-80-5
  N-Methyl-N-ethylcathinone H Me Me Et 1157739-24-6
  Bupropion 3-Cl Me H t-Bu 34911-55-2
  Hydroxybupropion 3-Cl Me H 2-Me-3-OH-propan-2-yl 357399-43-0
  Mephedrone 4-Me Me H Me 1189805-46-6
  2-MMC 2-Me Me H Me 1246911-71-6
  2-MEC 2-Me Me H Et 1439439-84-5
  2-EMC 2-Et Me H Me
  2-EEC 2-Et Me H Et 2446466-59-5
  3-MMC 3-Me Me H Me 1246816-62-5
  3-MEC 3-Me Me H Et 1439439-83-4
  3-MPC 3-Me Me H nPr
  3-EMC 3-Et Me H Me
  3-EEC 3-Et Me H Et 2446466-61-9
  4-EMC 4-Et Me H Me 1225622-14-9
  4-EEC 4-Et Me H Et 2446466-62-0
  4-MC 4-Me Me H H 31952-47-3
  Benzedrone 4-Me Me H Bn 1225617-75-3
  2'-MeO-Benzedrone 4-Me Me H 2-MeO-Bn
  2,N-Dimethylbenzedrone 2-Me Me Me Bn
  3,N-Dimethylbenzedrone 3-Me Me Me Bn
  4,N-Dimethylbenzedrone 4-Me Me Me Bn
  4-MEC 4-Me Me H Et 1225617-18-4
  4-MPC 4-Me Me H nPr
  N,N-DMMC 4-Me Me Me Me 1448845-14-4
  N,N-MEMC 4-Me Me Me Et
  N,N-DEMC 4-Me Me Et Et 676316-90-8
  4-MEAP 4-Me Pr H Et 746540-82-9
  EDMC 4-Et Me Me Me
  2,3-DMMC 2,3-dimethyl Me H Me
  2,3-DMEC 2,3-dimethyl Me H Et
  2,4-DMMC 2,4-dimethyl Me H Me 1225623-63-1
  2,4-DMEC 2,4-dimethyl Me H Et 1225913-88-1
  2,5-DMMC 2,5-dimethyl Me H Me
  2,5-DMEC 2,5-dimethyl Me H Et
  2,6-DMMC 2,6-dimethyl Me H Me
  2,6-DMEC 2,6-dimethyl Me H Et
  3,4-DMMC 3,4-dimethyl Me H Me 1082110-00-6
  3,4-DMEC 3,4-dimethyl Me H Et 1225811-81-3
  3,5-DMEC 3,5-dimethyl Me H Et
  2,4,5-TMMC 2,4,5-trimethyl Me H Me 1368603-85-3
  2,4,5-TMOMC 2,4,5-trimethoxy Me H Me
  3,4,5-TMOMC 3,4,5-trimethoxy Me H Me
  Methedrone 4-MeO Me H Me 530-54-1
  Dimethedrone 4-MeO Me Me Me 91564-39-5
  Ethedrone 4-MeO Me H Et
  2-MOMC 2-MeO Me H Me
  3-MOMC 3-MeO Me H Me 1435933-70-2
  3-FC 3-F Me H H 1082949-91-4
  4-FC 4-F Me H H 80096-51-1
  2-FMC 2-F Me H Me 1186137-35-8
  2-FEC 2-F Me H Et
  3-FMC 3-F Me H Me 1049677-77-1
  3-FEC 3-F Me H Et
  2-CMC 2-Cl Me H Me
  2-BMC 2-Br Me H Me
  2-IMC 2-I Me H Me
  2-TFMAP 2-CF3 Me H Me
  Clophedrone 3-Cl Me H Me 1049677-59-9
  3-CEC 3-Cl Me H Et 2150476-60-9
  3-BMC 3-Br Me H Me 676487-42-6
  3-IMC 3-I Me H Me
  3-TFMAP 3-CF3 Me H Me
  Flephedrone 4-F Me H Me 447-40-5
  4-FEC 4-F Me H Et 1225625-74-0
  Clephedrone 4-Cl Me H Me 1225843-86-6
  2-CEC 2-Cl Me H Et
  4-CEC 4-Cl Me H Et 14919-85-8
  2-CiPC 2-Cl Me H iPr
  3-CiPC 3-Cl Me H iPr
  4-CiPC 4-Cl Me H iPr
  4-CBC 4-Cl Me H nBu 1225621-71-5
  2-CDMC 2-Cl Me Me Me
  3-CDMC 3-Cl Me Me Me
  4-CDMC 4-Cl Me Me Me 1157667-29-2
  Brephedrone 4-Br Me H Me 486459-03-4
  4-BEC 4-Br Me H Et 135333-26-5
  4-IMC 4-I Me H Me
  4-TFMAP 4-CF3 Me H Me
  4-EFMC 4-(2-fluoroethyl) Me H Me
  4-MTMC 4-SCH3 Me H Me
  4-MSMC 4-SO2CH3 Me H Me
  4-PHMC 4-phenyl Me H Me
  Mexedrone 4-Me methoxymethyl H Me
  FMMC 3-F-4-Me Me H Me 1696642-00-8
  MFMC 3-Me-4-F Me H Me 1368943-21-8
  4-Cl-3-MMC 3-Me-4-Cl Me H Me
  MMOMC 3-Me-4-MeO Me H Me
  3,4-DCMC 3,4-dichloro Me H Me 802281-39-6
  3,4-DCEC 3,4-dichloro Me H Et 1225618-63-2
  3,5-DCMC 3,5-dichloro Me H Me
  3,5-DFMC 3,5-difluoro Me H Me 1430343-55-7
  2,5-DMOMC 2,5-dimethoxy Me H Me
  βk-2C-C 2,5-dimethoxy-4-chloro H H H 1538191-15-9
  βk-2C-B 2,5-dimethoxy-4-bromo H H H 807631-09-0
  βk-2C-I 2,5-dimethoxy-4-iodo H H H
  βk-2C-D 2,5-dimethoxy-4-methyl H H H 1368627-25-1
  βk-2C-E 2,5-dimethoxy-4-ethyl H H H 1517021-02-1
  βk-2C-P 2,5-dimethoxy-4-propyl H H H
  βk-2C-iP 2,5-dimethoxy-4-isopropyl H H H 1511033-62-7
  βk-DOB 2,5-dimethoxy-4-bromo Me H H
  βk-MDOM 2,5-dimethoxy-4-methyl Me H Me
  βk-MDA 3,4-methylenedioxy Me H H 80535-73-5
  N-Acetyl-βk-MDA 3,4-methylenedioxy Me H acetyl
  2,3-MDMC 2,3-methylenedioxy Me H Me 1427205-87-5
  Methylone 3,4-methylenedioxy Me H Me 186028-79-5
  Dimethylone 3,4-methylenedioxy Me Me Me 109367-07-9
  N-Acetylmethylone 3,4-methylenedioxy Me acetyl Me
  N-Hydroxymethylone 3,4-methylenedioxy Me hydroxy Me
  Ethylone 3,4-methylenedioxy Me H Et 1112937-64-0
  Diethylone 3,4-methylenedioxy Me Et Et
  N-Acetylethylone 3,4-methylenedioxy Me acetyl Et
  N-Isopropyl-βk-MDA 3,4-methylenedioxy Me H iPr
  MDPT 3,4-methylenedioxy Me H t-Bu 186028-84-2
  Benzylone (BMDP) 3,4-methylenedioxy Me H Bn 1823274-68-5
  N-Cyclohexylmethylone 3,4-methylenedioxy Me H cyclohexyl
  3,4-EDMC 3,4-ethylenedioxy Me H Me 30253-44-2
  βk-IMP 3,4-trimethylene Me H Me 100608-69-3
  βk-IBP 3,4-trimethylene Et H Et
  βk-IVP 3,4-trimethylene nPr H Et
  3-Fluorobuphedrone 3-F Et H Me
  4-Fluorobuphedrone 4-F Et H Me 1368599-12-5
  4-Bromobuphedrone 4-Br Et H Me
  3-Methylbuphedrone 3-Me Et H Me 1797911-07-9
  4-Me-MABP 4-Me Et H Me 1336911-98-8
  4-Me-NEB 4-Me Et H Et 18268-19-4
  2-F-NEB 2-F Et H Et
  3F-NEB 3-F Et H Et
  4-F-NEB 4-F Et H Et
  4-Me-DMB 4-Me Et Me Me
  3,4-DMEB 3,4-dimethyl Et H Et
  4-Methoxybuphedrone 4-MeO Et H Me
  Butylone 3,4-methylenedioxy Et H Me 802575-11-7
  Eutylone 3,4-methylenedioxy Et H Et 802855-66-9
  βk-PBDB 3,4-methylenedioxy Et H nPr
  Bn-4-MeMABP 4-Me Et H Bn 1445751-39-2
  BMDB 3,4-methylenedioxy Et H Bn 1445751-47-2
  N-Cyclohexylbutylone 3,4-methylenedioxy Et H cyclohexyl
  βk-DMBDB 3,4-methylenedioxy Et Me Me 802286-83-5
  βk-MMDMA 3,4-methylenedioxy-5-MeO Me H Me 2230716-98-8
  βk-MMDMA-2 2-MeO-3,4-methylenedioxy Me H Me
  βk-DMMDA 2,5-diMeO-3,4-methylenedioxy Me H H
  5-Methylmethylone 3,4-methylenedioxy-5-Me Me H Me 1364933-83-4
  5-Methylethylone 3,4-methylenedioxy-5-Me Me H Et 1364933-82-3
  2-Methylbutylone 2-Me-3,4-methylenedioxy Et H Me 1364933-86-7
  5-Methylbutylone 3,4-methylenedioxy-5-Me Et H Me 1354631-29-0
  Pentylone 3,4-methylenedioxy nPr H Me 698963-77-8
  N-Ethylpentylone 3,4-methylenedioxy nPr H Et 727641-67-0
  N-propylpentylone 3,4-methylenedioxy nPr H nPr
  N-butylpentylone 3,4-methylenedioxy nPr H nBu
  2,3-Dipentylone 2,3-methylenedioxy nPr Me Me
  Dipentylone 3,4-methylenedioxy nPr Me Me 17763-13-2
  N,N-Diethylnorpentylone 3,4-methylenedioxy nPr Et Et
  Hexylone 3,4-methylenedioxy nBu H Me
  Isohexylone 3,4-methylenedioxy iBu H Me 1157947-89-1
  Isoheptylone 3,4-methylenedioxy iPe H Me
  N-Ethylhexylone 3,4-methylenedioxy nBu H Et 27912-41-0
  N-Ethylheptylone 3,4-methylenedioxy nPe H Et
  4-MEAP 4-Me nPr H Et 746540-82-9
  3,4-DMEP 3,4-dimethyl nPr H Et
  2-F-Pentedrone 2-F nPr H Me
  3-F-Pentedrone 3-F nPr H Me
  4-F-Pentedrone 4-F nPr H Me
  4-Cl-Pentedrone 4-Cl nPr H Me 2167949-43-9
  4-Methylpentedrone 4-Me nPr H Me 1373918-61-6
  DL-4662 3,4-dimethoxy nPr H Et 1674389-55-9
  4-F-iPr-norpentedrone 4-F nPr H iPr
  3-CBV 3-Cl nPr H tBu
  4-methylhexedrone 4-Me nBu H Me
  MEH 4-Me nBu H Et
  3F-NEH 3-F nBu H Et
  4-F-hexedrone 4-F nBu H Me
  4-F-octedrone 4-F hexyl H Me
  α-phenylmephedrone 4-Me phenyl H Me
  βk-Ephenidine H phenyl H Et 22312-16-9
  BMAPN β-naphthyl instead of phenyl Me H Me
  βk-Methiopropamine thiophen-2-yl instead of phenyl Me H Me 24065-17-6
  5-Cl-bk-MPA 5-chlorothiophen-2-yl instead of phenyl Me H Me
  βk-5-MAPB benzofuran-5-yl instead of phenyl Me H Me
  βk-6-MAPB benzofuran-6-yl instead of phenyl Me H Me
  βk-5-IT indol-5-yl instead of phenyl Me H H 1369231-36-6
  βk-5F-NM-AMT[38] 5-fluoroindol-3-yl instead of phenyl Me H Me
  α-Phthalimidopropiophenone H Me phthalimido 19437-20-8
  PPPO H Me piperidinyl
  PPBO H Et piperidinyl 92728-82-0
  FPPVO 4-F nPr piperidinyl
  3,4-Pr-PipVP 3,4-trimethylene nPr piperidinyl
  MDPV-azepane 3,4-methylenedioxy nPr azepane
  Caccure 907 4-SCH3 α,α-di-Me morpholinyl
  α-PPP H Me pyrrolidinyl 19134-50-0
  α-PBP H Et pyrrolidinyl 13415-54-8
  α-PVP (O-2387) H nPr pyrrolidinyl 14530-33-7
  α-PHP H nBu pyrrolidinyl 13415-86-6
  α-PHiP H iBu pyrrolidinyl
  α-PEP (α-PHPP) H nPe pyrrolidinyl 13415-83-3
  α-POP H hexyl pyrrolidinyl
  α-PNP H heptyl pyrrolidinyl
  DPPE (Alpha-D2PV) H phenyl pyrrolidinyl 27590-61-0
  α-PcPeP H cyclopentyl pyrrolidinyl
  α-PCYP H cyclohexyl pyrrolidinyl 1803168-11-7
  2-MePPP 2-Me Me pyrrolidinyl 2092429-83-7
  3-MePPP 3-Me Me pyrrolidinyl 1214940-01-8
  4-MePPP 4-Me Me pyrrolidinyl 1313393-58-6
  3-MeO-PPP 3-MeO Me pyrrolidinyl
  MOPPP 4-MeO Me pyrrolidinyl 478243-09-3
  3-F-PPP 3-F Me pyrrolidinyl 1214939-99-7
  FPPP 4-F Me pyrrolidinyl 28117-76-2
  Cl-PPP 4-Cl Me pyrrolidinyl 93307-24-5
  3-Br-PPP 3-Br Me pyrrolidinyl
  Br-PPP 4-Br Me pyrrolidinyl
  2,3-DMPPP 2,3-dimethyl Me pyrrolidinyl
  2,4-DMPPP 2,4-dimethyl Me pyrrolidinyl
  3,4-DMPPP 3,4-dimethyl Me pyrrolidinyl
  3-MPBP 3-Me Et pyrrolidinyl 1373918-60-5
  3-F-PBP 3-F Et pyrrolidinyl 1373918-59-2
  MPBP 4-Me Et pyrrolidinyl 732180-91-5
  FPBP 4-F Et pyrrolidinyl 1373918-67-2
  EPBP 4-Et Et pyrrolidinyl
  MOPBP 4-MeO Et pyrrolidinyl
  MMOPBP 3-Me-4-MeO Et pyrrolidinyl
  O-2384 3,4-dichloro Et pyrrolidinyl 850352-65-7
  2-Me-PVP 2-Me nPr pyrrolidinyl 850352-54-4
  3-Me-PVP 3-Me nPr pyrrolidinyl 13415-85-5
  Pyrovalerone (O-2371) 4-Me nPr pyrrolidinyl 3563-49-3
  4-Et-PVP 4-Et nPr pyrrolidinyl
  3F-PVP 3-F nPr pyrrolidinyl 2725852-55-9
  FPVP 4-F nPr pyrrolidinyl 850352-31-7
  2-Cl-PVP 2-Cl nPr pyrrolidinyl
  3-Cl-PVP 3-Cl nPr pyrrolidinyl
  4-Cl-PVP 4-Cl nPr pyrrolidinyl 5537-17-7
  3-Br-PVP 3-Br nPr pyrrolidinyl
  4-Br-PVP 4-Br nPr pyrrolidinyl
  MOPVP 4-MeO nPr pyrrolidinyl 5537-19-9
  DMOPVP 3,4-dimethoxy nPr pyrrolidinyl 850442-84-1
  DMPVP 3,4-dimethyl nPr pyrrolidinyl
  O-2390 3,4-dichloro nPr pyrrolidinyl 850352-61-3
  MFPVP 3-methyl-4-fluoro nPr pyrrolidinyl
  MPHP 4-Me nBu pyrrolidinyl 34138-58-4
  3F-PHP 3-F nBu pyrrolidinyl
  4F-PHP 4-F nBu pyrrolidinyl 2230706-09-7
  4-Cl-PHP 4-Cl nBu pyrrolidinyl 2748592-29-0
  DMOPHP 3,4-dimethoxy nBu pyrrolidinyl
  MFPHP 3-Me-4-F nBu pyrrolidinyl
  3F-PiHP 3-F iBu pyrrolidinyl
  4F-PiHP 4-F iBu pyrrolidinyl
  O-2394 4-Me iBu pyrrolidinyl 850352-51-1
  MPEP 4-Me pentyl pyrrolidinyl
  4F-PV8 4-F pentyl pyrrolidinyl
  4-MeO-PV8 4-MeO pentyl pyrrolidinyl
  MFPEP 3-Me-4-F pentyl pyrrolidinyl
  MCPEP 3-Me-4-Cl pentyl pyrrolidinyl
  4F-PV9 4-F hexyl pyrrolidinyl
  4-MeO-PV9 4-MeO hexyl pyrrolidinyl
  α-Phenylpyrovalerone 4-Me phenyl pyrrolidinyl
  MDPPP 3,4-methylenedioxy Me pyrrolidinyl 783241-66-7
  MDMPP 3,4-methylenedioxy α,α-di-Me pyrrolidinyl
  MDPBP 3,4-methylenedioxy Et pyrrolidinyl 784985-33-7
  MDPV 3,4-methylenedioxy nPr pyrrolidinyl 687603-66-3
  2,3-MDPV 2,3-methylenedioxy nPr pyrrolidinyl
  5-Me-MDPV 3,4-methylenedioxy-5-Me nPr pyrrolidinyl
  6-Me-MDPV 2-Me-4,5-methylenedioxy nPr pyrrolidinyl
  6-MeO-MDPV 2-MeO-4,5-methylenedioxy nPr pyrrolidinyl
  Br-MeO-MDPV 2,3-methylenedioxy-4-MeO-5-Br nPr pyrrolidinyl
  MDPiVP 3,4-methylenedioxy iPr pyrrolidinyl
  MDPHP 3,4-methylenedioxy nBu pyrrolidinyl 776994-64-0
  MDPHiP 3,4-methylenedioxy iBu pyrrolidinyl
  MDPEP (MD-PV8) 3,4-methylenedioxy pentyl pyrrolidinyl 24646-39-7
  MDPOP (MD-PV9) 3,4-methylenedioxy hexyl pyrrolidinyl 24646-40-0
  3,4-EtPV 3,4-dimethylene nPr pyrrolidinyl
  5-PPDi 3,4-trimethylene Et pyrrolidinyl
  Indanyl-α-PVP 3,4-trimethylene nPr pyrrolidinyl 2748590-83-0
  5-BPDi 3,4-trimethylene nBu pyrrolidinyl
  IPPV 3,4-trimethylene phenyl pyrrolidinyl
  TH-PBP 3,4-tetramethylene Et pyrrolidinyl
  TH-PVP 3,4-tetramethylene nPr pyrrolidinyl 2304915-07-7
  TH-PHP 3,4-tetramethylene nBu pyrrolidinyl
  5-DBFPV 2,3-dihydrobenzofuran-5-yl instead of Ph nPr pyrrolidinyl 1620807-94-4
  3-BF-PVP benzofuran-3-yl instead of Ph nPr pyrrolidinyl
  Naphyrone (O-2482) β-naphthyl instead of phenyl nPr pyrrolidinyl 850352-53-3
  α-Naphyrone α-naphthyl instead of phenyl nPr pyrrolidinyl
  α-PPT thiophen-2-yl instead of phenyl Me pyrrolidinyl
  α-PBT thiophen-2-yl instead of phenyl Et pyrrolidinyl
  α-PVT thiophen-2-yl instead of phenyl nPr pyrrolidinyl 1400742-66-6

Legality

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On 2 April 2010, the Advisory Council on the Misuse of Drugs in the UK announced that a broad structure-based ban of this entire class of compounds would be instituted, following extensive publicity around grey-market sales and recreational use of mephedrone, a common member of the family. This ban covers compounds with the aforementioned general structure, with 28 compounds specifically named.[39]

"Any compound (not being bupropion or a substance for the time being specified in paragraph 2.2) structurally derived from 2-amino-1-phenyl-1-propanone by modification in any of the following ways, that is to say,

(i) by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents;

(ii) by substitution at the 3-position with an alkyl substituent;

(iii) by substitution at the nitrogen atom with alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure."

— ACMD, 2 April 2010

This text was added as an amendment to the Misuse of Drugs Act 1971, to come into force on 16 April 2010.[40] Note that four of the above compounds (cathinone, methcathinone, diethylpropion and pyrovalerone) were already illegal in the UK at the time the ACMD report was issued. Two compounds were specifically excluded from the ban, these being bupropion because of its common use in medicine and relative lack of abuse potential, and naphyrone because its structure falls outside the generic definition and not enough evidence was yet available to justify a ban.

Naphyrone analogues were subsequently banned in July 2010 following a further review by the ACMD,[41][42] along with a further broad based structure ban even more expansive than the last.[43][44]

"Any compound structurally derived from 2–aminopropan–1–one by substitution at the 1-position with any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), whether or not the compound is

further modified in any of the following ways, that is to say—

(i) by substitution in the ring system to any extent with alkyl, alkoxy, haloalkyl or halide substituents, whether or not further substituted in the ring system by one or more other univalent substituents;

(ii) by substitution at the 3–position with an alkyl substituent;

(iii) by substitution at the 2-amino nitrogen atom with alkyl or dialkyl groups, or

by inclusion of the 2-amino nitrogen atom in a cyclic structure".

— Home Office, 13 July 2010.
 
General chemical structure of substituted naphyrones, with R1-R3 defined in text

The substitutions in the general structure for naphyrone analogues subject to the ban may be described as follows:

  • Cyc = any monocyclic, or fused-polycyclic ring system (not being a phenyl ring or alkylenedioxyphenyl ring system), including analogues where the ring system is substituted to any extent with alkyl, alkoxy, haloalkyl or halide substituents, whether or not further substituted in the ring system by one or more other univalent substituents
  • R1 = hydrogen or any alkyl group
  • R2 = hydrogen, any alkyl group, or incorporation in a cyclic structure
  • R3 = hydrogen, any alkyl group, or incorporation in a cyclic structure

More new derivatives have however continued to appear, with the UK reporting more novel cathinone derivatives detected in 2010 than any other country in Europe, with most of them first identified after the generic ban had gone into effect and thus already being illegal despite never having been previously reported.[45]

In the United States, substituted cathinones are the psychoactive ingredients in "bath salts" which as of July 2011 were banned by at least 28 states, but not by the federal government.[46]

See also

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References

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  1. ^ Meltzer PC, Butler D, Deschamps JR, Madras BK (February 2006). "1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors". Journal of Medicinal Chemistry. 49 (4): 1420–32. doi:10.1021/jm050797a. PMC 2602954. PMID 16480278.
  2. ^ Paillet-Loilier M, Cesbron A, Le Boisselier R, Bourgine J, Debruyne D (2014). "Emerging drugs of abuse: current perspectives on substituted cathinones". Substance Abuse and Rehabilitation. 5: 37–52. doi:10.2147/SAR.S37257. PMC 4043811. PMID 24966713.
  3. ^ Simmons SJ, Leyrer-Jackson JM, Oliver CF, Hicks C, Muschamp JW, Rawls SM, Olive MF (October 2018). "DARK Classics in Chemical Neuroscience: Cathinone-Derived Psychostimulants". ACS Chemical Neuroscience. 9 (10): 2379–2394. doi:10.1021/acschemneuro.8b00147. PMC 6197900. PMID 29714473.
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  5. ^ Majchrzak M, Celiński R, Kuś P, Kowalska T, Sajewicz M (2018). "The newest cathinone derivatives as designer drugs: an analytical and toxicological review". Forensic Toxicology. 36 (1): 33–50. doi:10.1007/s11419-017-0385-6. PMC 5754390. PMID 29367861.
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