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Open Access Articles- Top Results for (-)-2%CE%B2-(1,2,4-Oxadiazol-5-methyl)-3%CE%B2-phenyltropane

(-)-2β-(1,2,4-Oxadiazol-5-methyl)-3β-phenyltropane

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(-)-2β-(1,2,4-Oxadiazol-5-methyl)-3β-phenyltropane
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Systematic (IUPAC) name
(1R,2S,3S,5S)-8-methyl-2-(3-methyl-1,2,4-oxadiazol-5-yl)-3-phenyl-8-azabicyclo[3.2.1]octane
Clinical data
  • Temporary Class Drug (NZ)
Identifiers
146659-37-2
Chemical data
Formula C17H21N3O
283.367 g/mol

RTI-126 ((–)-2β-(1,2,4-oxadiazol-5-methyl)-3β-phenyltropane) is a phenyltropane derivative which acts as a potent monoamine reuptake inhibitor and stimulant drug. It is around 5 times more potent a stimulant than cocaine, but is relatively unselective. It binds to all three monoamine transporters, although still with some selectivity for the dopamine transporter.[1] RTI-126 has a fast onset of effects and short duration of action, and its pharmacological profile in animals is among the closest to cocaine itself out of all the drugs in the RTI series. Its main application in scientific research has been in studies investigating the influence of pharmacokinetics on the abuse potential of stimulant drugs, with its rapid entry into the brain thought to be a key factor in producing its high propensity for development of dependence in animals.[2][3]


The structurally related compound (–)-2β-(3-methyl-5-isoxazolyl)nortropane is a potent and selective agonist for nicotinic acetylcholine receptors, with twice the potency of nicotine.[4]

File:2β-(3-methyl-5-isoxazolyl)nortropane structure.png
(–)-2β-(3-methyl-5-isoxazolyl)nortropane


See also

References

  1. ^ Carroll, FI; Gray, JL; Abraham, P; Kuzemko, MA; Lewin, AH; Boja, JW; Kuhar, MJ (1993). "3-Aryl-2-(3′-substituted-1′,2′,4′-oxadiazol-5′-yl)tropane analogues of cocaine: affinities at the cocaine binding site at the dopamine, serotonin, and norepinephrine transporters". Journal of Medical Chemistry 36 (20): 2886–90. PMID 8411004. doi:10.1021/jm00072a007. 
  2. ^ Kimmel, HL; Carroll, FI; Kuhar, MJ (2001). "Locomotor stimulant effects of novel phenyltropanes in the mouse". Drug and alcohol dependence 65 (1): 25–36. PMID 11714587. doi:10.1016/S0376-8716(01)00144-2. 
  3. ^ Kimmel, HL; O'Connor, JA; Carroll, FI; Howell, LL (2007). "Faster onset and dopamine transporter selectivity predict stimulant and reinforcing effects of cocaine analogs in squirrel monkeys". Pharmacology, Biochemistry, and Behavior 86 (1): 45–54. PMC 1850383. PMID 17258302. doi:10.1016/j.pbb.2006.12.006. 
  4. ^ Cheng J, Izenwasser S, Zhang C, Zhang S, Wade D, Trudell ML. Synthesis and nicotinic acetylcholine receptor binding affinities of 2- and 3-isoxazolyl-8-azabicyclo[3.2.1]octanes. Bioorganic and Medicinal Chemistry Letters. April 2004; 14(7):1775-1778. doi:10.1016/j.bmcl.2004.01.025 PMID 15026069

Template:Phenyltropanes


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