{"type":"standard","title":"SeDMA","displaytitle":"SeDMA","namespace":{"id":0,"text":""},"wikibase_item":"Q131298914","titles":{"canonical":"SeDMA","normalized":"SeDMA","display":"SeDMA"},"pageid":78003158,"thumbnail":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/c/c4/SeDMA.svg/330px-SeDMA.svg.png","width":320,"height":157},"originalimage":{"source":"https://upload.wikimedia.org/wikipedia/commons/thumb/c/c4/SeDMA.svg/530px-SeDMA.svg.png","width":530,"height":260},"lang":"en","dir":"ltr","revision":"1282725984","tid":"be5dc7a5-0b9f-11f0-aded-a250a1d565f5","timestamp":"2025-03-28T06:41:57Z","description":"MDMA analogue","description_source":"local","content_urls":{"desktop":{"page":"https://en.wikipedia.org/wiki/SeDMA","revisions":"https://en.wikipedia.org/wiki/SeDMA?action=history","edit":"https://en.wikipedia.org/wiki/SeDMA?action=edit","talk":"https://en.wikipedia.org/wiki/Talk:SeDMA"},"mobile":{"page":"https://en.m.wikipedia.org/wiki/SeDMA","revisions":"https://en.m.wikipedia.org/wiki/Special:History/SeDMA","edit":"https://en.m.wikipedia.org/wiki/SeDMA?action=edit","talk":"https://en.m.wikipedia.org/wiki/Talk:SeDMA"}},"extract":"SeDMA is a bioisosteric analogue of 3,4-methylenedioxy-N-methylamphetamine (MDMA) which was developed in an attempt to create an improved MDMA alternative for potential clinical use. It is the analogue of MDMA in which the 1,3-benzodioxole ring has been replaced with a 2,1,3-benzoselenadiazole ring. ODMA and TDMA are closely related analogues. ODMA, TDMA, and SeDMA are releasing agents of serotonin, norepinephrine, and dopamine similarly to MDMA. However, they are less potent and efficacious in activating the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors than MDMA and show differing and potentially improved metabolic and pharmacokinetic properties in comparison. ODMA, TDMA, and SeDMA were first described in the scientific literature in June 2024.","extract_html":"
SeDMA is a bioisosteric analogue of 3,4-methylenedioxy-N-methylamphetamine (MDMA) which was developed in an attempt to create an improved MDMA alternative for potential clinical use. It is the analogue of MDMA in which the 1,3-benzodioxole ring has been replaced with a 2,1,3-benzoselenadiazole ring. ODMA and TDMA are closely related analogues. ODMA, TDMA, and SeDMA are releasing agents of serotonin, norepinephrine, and dopamine similarly to MDMA. However, they are less potent and efficacious in activating the serotonin 5-HT2A, 5-HT2B, and 5-HT2C receptors than MDMA and show differing and potentially improved metabolic and pharmacokinetic properties in comparison. ODMA, TDMA, and SeDMA were first described in the scientific literature in June 2024.
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