3,4-Dichloromethylphenidate

Source: Wikipedia, the free encyclopedia.

3,4-DCMP
oral, insufflation, rectal
ATC code
  • none
Legal status
Legal status
Pharmacokinetic data
MetabolismPrimarily by the liver
ExcretionPredominantly renal
Identifiers
  • Methyl 2-(3,4-dichlorophenyl)-2-(piperidin-2-yl)acetate
JSmol)
SMILES
  • COC(=O)C(c1ccc(c(c1)Cl)Cl)C2CCCCN2
  • InChI=1S/C14H17Cl2NO2/c1-19-14(18)13(12-4-2-3-7-17-12)9-5-6-10(15)11(16)8-9/h5-6,8,12-13,17H,2-4,7H2,1H3 checkY
  • Key:JUKMAYKVHWKRKY-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

3,4-dichloromethylphenidate (abbreviated as 3,4-DCMP, and incorrectly as 3,4-CTMP for the d,l-threo diastereomer) is a potent stimulant drug from the phenidate class closely related to methylphenidate. It acts as a potent serotonin-norepinephrine-dopamine reuptake inhibitor with a long duration of action.[clarification needed] It has been sold online as a designer drug.[1][2]

Chemistry

3,4-DCMP is the 3,4-dichlorinated analogue of methylphenidate. The 3,4-dichlorination is a common modification done to most monoamine reuptake inhibitors.[citation needed]

Pharmacology

Pharmacodynamics

The result of the 3,4-dichlorination on 3,4-DCMP is a higher selectivity for the serotonin transporter and serotonin uptake inhibition. Serotonergic activity among phenidates is very rare, and 3,4-DCMP is one of only three compounds from this class with appreciable serotoninergic activity, the other two being HDMP-28 & HDEP-28. The reason for the serotoninergic activity of all three compounds is a bulky aryl ring system (in the case of the aforementioned compounds, a 2-naphthalene ring), which mimics the bicyclic indole ring system of serotonin. Examples of compounds with the same SAR modifications done to increase serotoninergic activity include naphthylaminopropane and 3,4-dichloroamphetamine.[citation needed]

The 3,4-dichloro group also increases resistance to metabolism, which can be seen on the compound's greatly increased duration of action and biological half-life. Furthermore, it also results in a greatly increased affinity for both the dopamine and noradrenaline transporters, because the 3,4-dichloro group more closely mimics the 3,4-dihydroxy group found on dopamine and adrenaline. Examples of compounds with the same SAR modification done to increase affinity to DAT & NET include dichloropane and O-2390.[citation needed]

3,4-CTMP, the d,l-threo diastereomer of 3,4-DCMP, is approximately seven times more potent than methylphenidate in animal studies, but has weaker reinforcing effects due to its slower onset of action.[2][3][4][5][6][7] However, H. M. Deutsch's discrimination ratio[clarification needed] implies it to be more reinforcing than cocaine.[5]

Inhibition of [125I]RTI-55 Binding and [3H]Monoamine Uptake of 3,4-DCMP diastereomers, and related compounds.[2]
Compound DAT

(Ki, nM)

DA uptake

IC50 (nM)

SERT

(Ki, nM)

5HT uptake

IC50 (nM)

NET

(Ki, nM)

NE uptake

IC50 (nM)

NET/DAT

selectivity

NE/DA uptake

selectivity

3,4-CTMP 1.4 ± 0.1 23 ± 3 1,600 ± 150 540 ± 110 14 ± 6 10 ± 1 10.0 0.43
3,4-CEMP1 90 ± 14 800 ± 110 2,500 ± 420 1,100 ± 90 4,200 ± 1,900 190 ± 50 46.7 0.24
TMP2 110 ± 9 110 ± 9 65,000 ± 4,000 5,100 ± 7,000 660 ± 50 61 ± 14 6.0 0.77
Cocaine 500 ± 65 240 ± 15 340 ± 40 250 ± 40 500 ± 90 210 ± 30 1.0 0.88
  • 1 This is an abbreviation of the d,l-erythro diastereomer of 3,4-DCMP.
  • 2 This is an abbreviation of d,l-threomethylphenidate, more widely known by its brand name Ritalin.

Legality

As of October 2015 3,4-CTMP is a controlled substance in China.[8]

3,4-CTMP was banned in the UK as a

Temporary Class Drug from April 2015 following its unapproved sale as a designer drug.[9]

Sweden's public health agency suggested to classify 3,4-CTMP as hazardous substance on 10 November 2014.[10]

See also

References

  1. ^ Wood S (10 April 2015). "Temporary Class Drug Order – legal highs' bubble to be 'burst'". Criminal Law Blog: Kingsley Napley.
  2. ^
    PMID 17228864
    .
  3. S2CID 26220081
    .
  4. PMID 8632426
    .
  5. ^
    PMID 11961053
    .
  6. PMID 17489581
    .
  7. PMID 10037500
    .
  8. ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
  9. ^ Methylphenidate-based NPS: A review of the evidence of use and harm. Advisory Council on the Misuse of Drugs, 31 March 2015
  10. ^ "Cannabinoider föreslås bli klassade som hälsofarlig vara". Retrieved 29 June 2015.
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