Difference between revisions of "25I-NBMD"
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Latest revision as of 21:04, 29 July 2010
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Systematic (IUPAC) name | |
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2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2,3-methylenedioxyphenyl)methyl]ethanamine | |
Chemical data | |
Formula | C18H20INO4 |
Molar mass | 441.259 g/mol[[Script error: No such module "String".]] |
Script error: No such module "collapsible list". | |
25I-NBMD (NBMD-2C-I) is a derivative of the phenethylamine hallucinogen 2C-I, discovered in 2006 by a team at Purdue University led by David Nichols. It acts as a potent agonist for the 5HT2A receptor with a Ki of 0.049nM at the human 5HT2A receptor.[1][2]
See also
- 2CBCB-NBOMe (NBOMe-TCB-2)
- 2CBFly-NBOMe (NBOMe-2CB-Fly)
- 25B-NBOMe (NBOMe-2CB)
- 25I-NBOH (NBOH-2CI)
- 25I-NBOMe (NBOMe-2CI)
References
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35px | This psychedelics, dissociatives and deliriants-related article is a stub. You can help ssf by expanding it. |
- ↑ Braden MR, Parrish JC, Naylor JC, Nichols DE. Molecular interaction of serotonin 5-HT2A receptor residues Phe339(6.51) and Phe340(6.52) with superpotent N-benzyl phenethylamine agonists. Molecular Pharmacology. 2006 Dec;70(6):1956-64. PMID 17000863
- ↑ Michael Robert Braden PhD. Towards a biophysical understanding of hallucinogen action. Purdue University 2007.
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