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25I-NBMD

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
25I-NBMD
Clinical data
Other namesNBMD-2C-I; Cimbi-29
Legal status
Legal status
Identifiers
  • N-[(2H-1,3-benzodioxol-4-yl)methyl]-2-(4-iodo-2,5-dimethoxyphenyl)ethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H20INO4
Molar mass441.265 g·mol−1
3D model (JSmol)
  • c13OCOc3cccc1CNCCc(c(OC)cc2I)cc2OC
  • InChI=1S/C18H20INO4/c1-21-16-9-14(19)17(22-2)8-12(16)6-7-20-10-13-4-3-5-15-18(13)24-11-23-15/h3-5,8-9,20H,6-7,10-11H2,1-2H3 checkY
  • Key:NJNMIPDEUMTYNV-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

25I-NBMD (NBMD-2C-I,Cimbi-29) is a derivative of thephenethylaminehallucinogen2C-I, discovered in 2006 by a team atPurdue University led byDavid Nichols. It acts as a potentpartial agonist for the5HT2Areceptor with aKi of 0.049 nM at the human 5HT2A receptor.[1][2][3] The corresponding 4-bromo analogue 25B-NBMD has been used for molecular dynamics studies on the shape of the 5-HT2A receptor.[4]

Society and culture

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Legality

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Sweden

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The Riksdag added 25I-NBMD toNarcotic Drugs Punishments Act underswedish schedule I ("substances, plant materials and fungi which normally do not have medical use") as of January 16, 2015, published byMedical Products Agency (MPA) in regulationLVFS 2014:11 listed as 25I-NBMD, and 2-(4-jodo-2,5-dimetoxifenyl)-N-[(2,3-metylendioxifenyl)metyl]etanamin.[5]

United Kingdom

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This substance is aClass A drug in the United Kingdom as a result of theN-benzylphenethylamine catch-all clause in theMisuse of Drugs Act 1971.[6]

See also

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References

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  1. ^Braden MR, Parrish JC, Naylor JC, Nichols DE (December 2006). "Molecular interaction of serotonin 5-HT2A receptor residues Phe339(6.51) and Phe340(6.52) with superpotent N-benzyl phenethylamine agonists".Molecular Pharmacology.70 (6):1956–64.doi:10.1124/mol.106.028720.PMID 17000863.S2CID 15840304.
  2. ^Braden MR (2007).Towards a biophysical understanding of hallucinogen action (Ph.D. thesis). Purdue University.ProQuest 304838368.
  3. ^Ettrup A, Hansen M, Santini MA, Paine J, Gillings N, Palner M, et al. (April 2011). "Radiosynthesis and in vivo evaluation of a series of substituted 11C-phenethylamines as 5-HT (2A) agonist PET tracers".European Journal of Nuclear Medicine and Molecular Imaging.38 (4):681–93.doi:10.1007/s00259-010-1686-8.PMID 21174090.S2CID 12467684.
  4. ^Isberg V, Balle T, Sander T, Jørgensen FS, Gloriam DE (February 2011). "G protein- and agonist-bound serotonin 5-HT2A receptor model activated by steered molecular dynamics simulations".Journal of Chemical Information and Modeling.51 (2):315–25.doi:10.1021/ci100402f.PMID 21261291.
  5. ^"Föreskrifter om ändring i Läkemedelsverkets föreskrifter (LVFS 2011:10) om förteckningar över narkotika" [Regulations amending the Medical Products Agency's regulations (LVFS 2011:10) on lists of narcotics](PDF) (in Swedish). Archived fromthe original(PDF) on 2015-03-16. Retrieved2017-04-21.
  6. ^"The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014".UK Statutory Instruments 2014 No. 1106. www.legislation.gov.uk.
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres:JRT
Others
Natural sources
5-HT1
5-HT1A
5-HT1B
5-HT1D
5-HT1E
5-HT1F
5-HT2
5-HT2A
5-HT2B
5-HT2C
5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Phenethylamines
Amphetamines
Phentermines
Cathinones
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(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
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