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Details

Stereochemistry RACEMIC
Molecular Formula C11H15NO.ClH
Molecular Weight 213.704
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEPHEDRONE HYDROCHLORIDE

SMILES

Cl.CNC(C)C(=O)C1=CC=C(C)C=C1

InChI

InChIKey=DLQZFTUKJGRPLZ-UHFFFAOYSA-N
InChI=1S/C11H15NO.ClH/c1-8-4-6-10(7-5-8)11(13)9(2)12-3;/h4-7,9,12H,1-3H3;1H

HIDE SMILES / InChI

Molecular Formula C11H15NO
Molecular Weight 177.2429
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Mephedrone (4-methylmethcathinone) is a β-ketoamphetamine belonging to the family of synthetic cathinones, an emerging class of designer drugs known for their hallucinogenic and psychostimulant properties as well as for their abuse potential. Mephedrone is a stimulant of dopamine (DA) release and blocks its reuptake through its interaction with the dopamine transporter. Furthermore, it has some affinity for various 5-hydroxytryptamine (5-HT) receptor subtypes. Neurotoxic effect of mephedrone on 5-HT and DA systems remains controversial. Although some studies in animal models reported no damage to DA nerve endings in the striatum and no significant changes in brain monoamine levels, some others suggested a rapid reduction in 5-HT and DA transporter function. Persistent serotonergic deficits were observed after binge like treatment in a warm environment and in both serotonergic and dopaminergic nerve endings at high ambient temperature. Oxidative stress cytotoxicity and an increase in frontal cortex lipid peroxidation were also reported. Despite the re-classification of mephedrone as a Class B restricted substance by the United Kingdom and restrictive legislation by the United States, international policy regarding mephedrone control is still developing and interest in synthetic amphetamine-like drugs could drive the development of future mephedrone analogues.

Approval Year

PubMed

PubMed

TitleDatePubMed
Neuronal changes and oxidative stress in adolescent rats after repeated exposure to mephedrone.
2015-07-01
Mephedrone toxicity in a Scottish emergency department.
2011-12
Mephedrone: use, subjective effects and health risks.
2011-11
Instability of the ecstasy market and a new kid on the block: mephedrone.
2011-11
Clinical characteristics of mephedrone toxicity reported to the U.K. National Poisons Information Service.
2011-08
[Mephedrone -- an old-new drug of abuse].
2011-07-24
Emergency department visits after use of a drug sold as "bath salts"--Michigan, November 13, 2010-March 31, 2011.
2011-05-20
Mephedrone (4-methylmethcathinone)-related deaths.
2011-04
Clinical pattern of toxicity associated with the novel synthetic cathinone mephedrone.
2011-04
Drugs for youth via Internet and the example of mephedrone.
2011-03-25
A case of extreme agitation and death after the use of mephedrone in The Netherlands.
2011-03-20
Mephedrone, new kid for the chop?
2011-01
Khat use and monitoring drug use in Europe: the current situation and issues for the future.
2010-12-01
Headshop heartache: acute mephedrone 'meow' myocarditis.
2010-12
Mephedrone: still available and twice the price.
2010-11-06
Dependence and psychosis with 4-methylmethcathinone (mephedrone) use.
2010-11-03
Case series of individuals with analytically confirmed acute mephedrone toxicity.
2010-11
Mephedrone use and associated adverse effects in school and college/university students before the UK legislation change.
2010-11
Methaemoglobinaemia due to mephedrone ('snow').
2010-10-22
The detection of mephedrone (4-methylmethcathinone) in 4 fatalities in Scotland.
2010-10-10
The serotonin syndrome as a result of mephedrone toxicity.
2010-09-20
Recreational use of mephedrone (4-methylmethcathinone, 4-MMC) with associated sympathomimetic toxicity.
2010-09
A harmless high?
2010-08-28
Analyses of second-generation 'legal highs' in the UK: initial findings.
2010-08
An analysis of the 'legal high' mephedrone.
2010-07-15
Second generation mephedrone. The confusing case of NRG-1.
2010-07-06
Britain moves to curtail new drug craze.
2010-06-15
Metabolism of designer drugs of abuse: an updated review.
2010-06-01
Beta-keto amphetamines: studies on the metabolism of the designer drug mephedrone and toxicological detection of mephedrone, butylone, and methylone in urine using gas chromatography-mass spectrometry.
2010-06
[Mephedrone: a designer drug of recent use in France].
2010-05-25
Head shop compound abuse amongst attendees of the Drug Treatment Centre Board.
2010-05
UK places generic ban on mephedrone drug family.
2010-04-17
A collapse in integrity of scientific advice in the UK.
2010-04-17
Chemical analysis of four capsules containing the controlled substance analogues 4-methylmethcathinone, 2-fluoromethamphetamine, alpha-phthalimidopropiophenone and N-ethylcathinone.
2010-04-15
Multiple-drug toxicity caused by the coadministration of 4-methylmethcathinone (mephedrone) and heroin.
2010-04
Home secretary bans mephedrone after taking advice from depleted council.
2010-03-31
Mephedrone is an amphetamine "by another name," drug adviser tells MPs.
2010-03-24
What should be done about mephedrone?
2010-03-23
[Mephedrone: A designer drug legally available on the Web].
2010-03-15
[Smoking by people addicted to drugs].
2010
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 20:35:19 GMT 2025
Edited
by admin
on Mon Mar 31 20:35:19 GMT 2025
Record UNII
G0XL35SUXP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEPHEDRONE HYDROCHLORIDE
Common Name English
1-PROPANONE, 2-(METHYLAMINO)-1-(4-METHYLPHENYL)-, HYDROCHLORIDE (1:1)
Preferred Name English
Code System Code Type Description
FDA UNII
G0XL35SUXP
Created by admin on Mon Mar 31 20:35:19 GMT 2025 , Edited by admin on Mon Mar 31 20:35:19 GMT 2025
PRIMARY
PUBCHEM
46782120
Created by admin on Mon Mar 31 20:35:19 GMT 2025 , Edited by admin on Mon Mar 31 20:35:19 GMT 2025
PRIMARY
CAS
1189726-22-4
Created by admin on Mon Mar 31 20:35:19 GMT 2025 , Edited by admin on Mon Mar 31 20:35:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID30922822
Created by admin on Mon Mar 31 20:35:19 GMT 2025 , Edited by admin on Mon Mar 31 20:35:19 GMT 2025
PRIMARY
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ACTIVE MOIETY