DIMENOXADOL

Dimenoxadol
Clinical data
Other names	Dimenoxadol, Estocin
ATC code	none;
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class A1 (Narcotic drugs); CA: Schedule I; DE: Anlage I (Authorized scientific use only); US: Schedule I; UN: Psychotropic Schedule I;
Identifiers
	IUPAC name 2-(dimethylamino)ethyl 2-ethoxy-2,2-diphenylacetate;
CAS Number	509-78-4 ;
PubChem CID	17036;
DrugBank	DB01461 ;
ChemSpider	16137 ;
UNII	4D65PBX0VK;
KEGG	D12672 ;
ChEMBL	ChEMBL2104309;
CompTox Dashboard ( EPA)	DTXSID5057759 ;
Chemical and physical data
Formula	C20H25NO3
Molar mass	327.424 g·mol−1
3D model ( JSmol)	Interactive image;
	SMILES CCOC(C1=CC=CC=C1)(C2=CC=CC=C2)C(=O)OCCN(C)C;
	InChI InChI=1S/C20H25NO3/c1-4-24-20(17-11-7-5-8-12-17,18-13-9-6-10-14-18)19(22)23-16-15-21(2)3/h5-14H,4,15-16H2,1-3H3 ; Key:RHUWRJWFHUKVED-UHFFFAOYSA-N ;
	(verify)

Dimenoxadol ( INN) (brand name Estocin (in Russia)), or dimenoxadole ( BAN), is an opioid analgesic which is a benzilic acid derivative, closely related to benactyzine (an anticholinergic). Further, the structure is similar to methadone and related compounds like dextropropoxyphene.

It was invented in Germany in the 1950s,^[2] and produces similar effects to other opioids, including analgesia, sedation, dizziness and nausea.^[3]^[4]^[5]

In the United States it is a Schedule I Narcotic controlled substance with an ACSCN of 9617 and a 2013 annual aggregate manufacturing quota of zero.

References

^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
^ GB 716700, Boehringer A, et al., "A new and improved analgesic and process for its production", published 10/13/1954
^ Gorbatova EN (1967). "[The pharmacology of estocin, an new analgesic]". Stomatologiia. 46 (2): 22–5. PMID 5232927.
^ Kingisepp GI, Kurvits K, Nurmand LB (1969). "[Pharmacology of dimethylaminoethyl ester of diphenylethoxyacetic acid hydrochloride--estocin]". Farmakologiia I Toksikologiia. 32 (6): 710–2. PMID 5381602.
^ Liberman SS (1968). "[Analgesic action of estocin (dimethylaminoethyl ester hydrochloride of alpha, alpha-diphenylethoxyacetic acid)]". Farmakologiia I Toksikologiia. 31 (6): 668–71. PMID 5729519.

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