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DOB-FLY

From Wikipedia, the free encyclopedia
Psychedelic drug
Not to be confused withBromo-DragonFLY.
Pharmaceutical compound
DOB-FLY
Clinical data
Other names3C-B-FLY; B-FLY
Legal status
Legal status
  • In general unscheduled
Identifiers
  • 1-(4-bromo-2,3,6,7-tetrahydrofuro[2,3-f][1]benzofuran-8-yl)propan-2-amine
CAS Number
PubChemCID
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Chemical and physical data
FormulaC13H16BrNO2
Molar mass298.180 g·mol−1
3D model (JSmol)
  • CC(CC1=C2CCOC2=C(C3=C1OCC3)Br)N
  • InChI=1S/C13H16BrNO2/c1-7(15)6-10-8-2-4-17-13(8)11(14)9-3-5-16-12(9)10/h7H,2-6,15H2,1H3
  • Key:FKRREVSELFOLDT-UHFFFAOYSA-N

DOB-FLY, also known as3C-B-FLY, is apsychedelic drug anddesigner drug of thephenethylamine,DOx, andFLY families that was developed byDavid E. Nichols and colleagues atPurdue University. It can be regarded as the α-methyl derivative of2C-B-FLY or the partially saturated counterpart ofBromo-DragonFLY. Unlike Bromo-DragonFLY, DOB-FLY is only slightly more potent thanDOB itself, with an active dose in humans of around 1 mg.[1][2][3][4][5][6]

See also

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References

[edit]
  1. ^Parker MA, Marona-Lewicka D, Lucaites VL, Nelson DL, Nichols DE (December 1998). "A novel (benzodifuranyl)aminoalkane with extremely potent activity at the 5-HT2A receptor".Journal of Medicinal Chemistry.41 (26):5148–9.doi:10.1021/jm9803525.PMID 9857084.
  2. ^Feng Z, Mohapatra S, Klimko PG, Hellberg MR, May JA, Kelly C, et al. (June 2007). "Novel benzodifuran analogs as potent 5-HT2A receptor agonists with ocular hypotensive activity".Bioorganic & Medicinal Chemistry Letters.17 (11):2998–3002.doi:10.1016/j.bmcl.2007.03.073.PMID 17419053.
  3. ^Parker MA, Kurrasch DM, Nichols DE (April 2008)."The role of lipophilicity in determining binding affinity and functional activity for 5-HT2A receptor ligands".Bioorganic & Medicinal Chemistry.16 (8):4661–9.doi:10.1016/j.bmc.2008.02.033.PMC 2442558.PMID 18296055.
  4. ^Schultz DM, Prescher JA, Kidd S, Marona-Lewicka D, Nichols DE, Monte A (June 2008)."'Hybrid' benzofuran-benzopyran congeners as rigid analogs of hallucinogenic phenethylamines".Bioorganic & Medicinal Chemistry.16 (11):6242–51.doi:10.1016/j.bmc.2008.04.030.PMC 2601679.PMID 18467103.
  5. ^Zaitsu K, Katagi M, Kamata H, Nakanishi K, Shima N, Kamata T, et al. (January 2010). "Simultaneous analysis of six novel hallucinogenic (tetrahydrobenzodifuranyl) aminoalkanes (FLYs) and (benzodifuranyl) aminoalkanes (DragonFLYs) by GC-MS, LC-MS, and LC-MS-MS".Forensic Toxicology.28 (1):9–18.doi:10.1007/s11419-009-0083-0.S2CID 24100422.
  6. ^Halberstadt AL, Chatha M, Stratford A, Grill M, Brandt SD (January 2019)."Comparison of the behavioral responses induced by phenylalkylamine hallucinogens and their tetrahydrobenzodifuran ("FLY") and benzodifuran ("DragonFLY") analogs".Neuropharmacology.144:368–376.doi:10.1016/j.neuropharm.2018.10.037.PMC 6863604.PMID 30385253.
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