Dimethylone (βk-MDDMA) is a substituted cathinone derivative with stimulant and empathogenic effects. Unlike the corresponding amphetamine derivative MDDM which is thought to be practically inactive, dimethylone substitutes for methamphetamine and MDMA in animal studies and has been sold as a designer drug.

Dimethylone | C12H15NO3 | CID 9794472 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities ...

Substituted cathinones are synthetic analogs of cathinone that can be considered as derivatives of phenethylamines with a beta-keto group on the side chain. They appeared in the recreational drug market in the mid-2000s and now represent a large ...

Methylone, also known as 3,4-methylenedioxy-N-methylcathinone (MDMC), is an entactogen and stimulant drug of the amphetamine, cathinone, and benzodioxole families related to 3,4-methylenedioxymethamphetamine (MDMA; "ecstasy"). [5] [1] [6] It is the β-keto or cathinone analogue of MDMA.[6] [1] Methylone is usually taken orally, but is also used by other routes.[5] …

2019年6月1日 · N-Ethylpentylone, dimethylone, dibutylone and clephedrone substituted fully for the discriminative stimulus effects of methamphetamine. N-Ethylpentylone, dibutylone and clephedrone fully substituted for cocaine, whereas dimethylone produced a maximum of 67% drug-appropriate responding. Dimethylone, dibutylone and clephedrone fully substituted ...

DIMETHYLONE 4G26NSP297 Other Structure General Names 6: Classification 1: Identifiers 4: Related Substances 2: DIMETHYLONE 4G26NSP297 Other Details Stereochemistry: RACEMIC Molecular Formula: C12H15NO3: Molecular Weight: 221.2524: Optical Activity ...

ChemSpider record containing structure, synonyms, properties, vendors and database links for DIMETHYLONE, 765231-58-1, OSNIIMCBVLBNGS-UHFFFAOYSA-N

DIMETHYLONE 4G26NSP297 Other Structure Moieties 1: General Record Details Names 6: Classification 1: Identifiers 4: Relationships 1: Active Moiety 1: DIMETHYLONE 4G26NSP297 Other Details Stereochemistry: RACEMIC ...

The shorter carbon tail caused lower affinity and potency at all three transporters. Dimethylone, with 2 methyl groups on the nitrogen and a short 1 carbon tail (Fig 1C, R 3), had the lowest affinities and potencies of the pentylone group, with all parameters in the micromolar range .

DIMETHYLONE HYDROCHLORIDE PEG3NSV0FB Other Structure General Names 5: Identifiers 3: Related Substances 2: DIMETHYLONE HYDROCHLORIDE PEG3NSV0FB Other Details Stereochemistry: RACEMIC Molecular Formula: C12H15NO3.ClH: Molecular Weight: 257.713: Optical Activity ...