Mesocarb

Mesocarb

Clinical data
Routes of administration	Oral
ATC code	none
Legal status
Legal status	CA: Schedule III DE: Anlage II (Prohibited) UK: Class C
Pharmacokinetic data
Metabolism	hepatic
Excretion	renal
Identifiers
IUPAC name 5-(Phenylcarbamoylimino)-3-(1-phenylpropan-2-yl)-5H-1,2,3-oxadiazol-3-ium-2-ide
CAS Number	34262-84-5 Y
PubChem CID	71932
ChemSpider	16736988 Y
UNII	UMT8MP2NDU
Chemical and physical data
Formula	C18H18N4O2
Molar mass	322.36 g/mol
3D model (Jmol)	Interactive image
SMILES O=C(\N=C1/C=[N+](\[N-]O1)C(C)Cc2ccccc2)Nc3ccccc3
InChI InChI=1S/C18H18N4O2/c1-14(12-15-8-4-2-5-9-15)22-13-17(24-21-22)20-18(23)19-16-10-6-3-7-11-16/h2-11,13-14H,12H2,1H3,(H,19,23)/b20-17+ Y Key:DMHQLXUFCQSQQQ-LVZFUZTISA-N Y

Mesocarb (brand names Sidnocarb, Sydnocarb) is a stimulant drug which was developed in the USSR in the 1970s. It has been found to act as a selective dopamine reuptake inhibitor, and is less potent and slower-acting but longer-lasting than dextroamphetamine.

Mesocarb was used for a variety of applications; these include counteracting the sedative effects of benzodiazepine drugs, increasing workload capacity and cardiovascular function, treatment of ADHD and hyperactivity in children, as a nootropic, and as a drug to enhance resistance to extremely cold temperatures. It is also listed as having antidepressant and anticonvulsant properties.

Mesocarb was sold in Russia as 5 milligram tablets under the brand name Sydnocarb. Hydroxylated metabolites can be detected in urine for up to 10 days after consumption.

Mesocarb is almost unknown in the western world and is neither used in medicine or studied scientifically to any great extent outside Russia and other countries in the former Soviet Union. It has however been added to the list of drugs under international control and is illegal in most countries, despite its multiple therapeutic applications and reported lack of significant abuse potential.

Mesocarb has been referred to as a prodrug of amphetamine. Indeed, it produces amphetamine as a metabolite, and amphetamine concentrations are far higher than mesocarb concentrations in human urine 22 hours post-administration (0.7–186 ng/mL and 0.004–0.17 ng/mL, respectively). However, mesocarb also possesses molecular actions of its own, inhibiting the reuptake of dopamine and to a far lesser extent of norepinephrine, but not of serotonin.

Mesocarb is a mesoionic sydnone imine. It has the amphetamine-backbone present, except that the R_N has a complicated imine side-chain present.