Open Access Articles- Top Results for UB-165


Systematic (IUPAC) name
Clinical data
200432-86-6 7pxY
PubChem CID 5310970
Chemical data
Formula C13H15ClN2
 14pxY (what is this?)  (verify)

UB-165 is a drug which acts as an agonist at neuronal nicotinic acetylcholine receptors being a full agonist of the α3β2 isoform and a partial agonist of the α4β2* isoform. It is used to study the role of this receptor subtype in the release of dopamine and noradrenaline in the brain,[1][2] and has also been used as a lead compound to derive a number of other selective nicotinic receptor ligands.[3][4][5][6]


  1. ^ Sharples, C. G.; Kaiser, P.; Soliakov, L.; Marks, M. J.; Collins, A. C.; Washburn, M.; Wright, E.; Spencer, J. A.; Gallagher, T.; Whiteaker, P.; Wonnacott, S. (2000). "UB-165: a novel nicotinic agonist with subtype selectivity implicates the alpha4beta2* subtype in the modulation of dopamine release from rat striatal synaptosomes". Journal of Neuroscience 20 (8): 2783–2791. PMID 10751429.  edit
  2. ^ Cao, Y.; Surowy, C.; Puttfarcken, P. (2005). "Nicotinic acetylcholine receptor-mediated 3Hdopamine release from hippocampus". The Journal of Pharmacology and Experimental Therapeutics 312 (3): 1298–1304. PMID 15542623. doi:10.1124/jpet.104.076794.  edit
  3. ^ Gohlke, H.; Gündisch; Schwarz; Seitz; Tilotta; Wegge (2002). "Synthesis and nicotinic binding studies on enantiopure diazine analogues of the novel (2-chloro-5-pyridyl)-9-azabicyclo4.2.1non-2-ene UB-165". Journal of Medicinal Chemistry 45 (5): 1064–1072. PMID 11855986. doi:10.1021/jm010936y.  edit
  4. ^ Sharples, C. G.; Karig; Simpson; Spencer; Wright; Millar; Wonnacott; Gallagher (2002). "Synthesis and pharmacological characterization of novel analogues of the nicotinic acetylcholine receptor agonist (+/-)-UB-165". Journal of Medicinal Chemistry 45 (15): 3235–3245. PMID 12109907. doi:10.1021/jm020814l.  edit
  5. ^ Sutherland, A.; Gallagher, T.; Sharples, C.; Wonnacott, S. (2003). "Synthesis of two fluoro analogues of the nicotinic acetylcholine receptor agonist UB-165". The Journal of Organic Chemistry 68 (6): 2475–2478. PMID 12636420. doi:10.1021/jo026698b.  edit
  6. ^ Karig, G.; Large; Sharples; Sutherland; Gallagher; Wonnacott (2003). "Synthesis and nicotinic binding of novel phenyl derivatives of UB-165. Identifying factors associated with alpha7 selectivity". Bioorganic & Medicinal Chemistry Letters 13 (17): 2825–2828. PMID 14611837. doi:10.1016/S0960-894X(03)00594-8.  edit

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