PROFILPELAJAR.COM

UB-165
Identifiers
	IUPAC name (1R,6R)-5-(6-chloropyridin-3-yl)-9-azabicyclo[4.2.1]non-4-ene;
CAS Number	200432-86-6 ;
PubChem CID	5310970;
CompTox Dashboard (EPA)	DTXSID401028829 ;
Chemical and physical data
Formula	C13H15ClN2
Molar mass	234.73 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES c2nc(Cl)ccc2C1=CCCC3CCC1N3;
	(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]

References

^ Sharples CG, Kaiser S, Soliakov L, Marks MJ, Collins AC, Washburn M, et al. (April 2000). "UB-165: a novel nicotinic agonist with subtype selectivity implicates the alpha4beta2* subtype in the modulation of dopamine release from rat striatal synaptosomes". The Journal of Neuroscience. 20 (8): 2783–91. doi:10.1523/JNEUROSCI.20-08-02783.2000. PMC 6772190. PMID 10751429.
^ Cao YJ, Surowy CS, Puttfarcken PS (March 2005). "Nicotinic acetylcholine receptor-mediated [3H]dopamine release from hippocampus". The Journal of Pharmacology and Experimental Therapeutics. 312 (3): 1298–304. doi:10.1124/jpet.104.076794. PMID 15542623. S2CID 20437091.
^ Gohlke H, Gündisch D, Schwarz S, Seitz G, Tilotta MC, Wegge T (February 2002). "Synthesis and nicotinic binding studies on enantiopure diazine analogues of the novel (2-chloro-5-pyridyl)-9-azabicyclo[4.2.1]non-2-ene UB-165". Journal of Medicinal Chemistry. 45 (5): 1064–72. doi:10.1021/jm010936y. PMID 11855986.
^ Sharples CG, Karig G, Simpson GL, Spencer JA, Wright E, Millar NS, et al. (July 2002). "Synthesis and pharmacological characterization of novel analogues of the nicotinic acetylcholine receptor agonist (+/-)-UB-165". Journal of Medicinal Chemistry. 45 (15): 3235–45. doi:10.1021/jm020814l. PMID 12109907.
^ Sutherland A, Gallagher T, Sharples CG, Wonnacott S (March 2003). "Synthesis of two fluoro analogues of the nicotinic acetylcholine receptor agonist UB-165". The Journal of Organic Chemistry. 68 (6): 2475–8. doi:10.1021/jo026698b. PMID 12636420.
^ Karig G, Large JM, Sharples CG, Sutherland A, Gallagher T, Wonnacott S (September 2003). "Synthesis and nicotinic binding of novel phenyl derivatives of UB-165. Identifying factors associated with alpha7 selectivity". Bioorganic & Medicinal Chemistry Letters. 13 (17): 2825–8. doi:10.1016/S0960-894X(03)00594-8. PMID 14611837.

[1] Sharples CG, Kaiser S, Soliakov L, Marks MJ, Collins AC, Washburn M, et al. (April 2000). "UB-165: a novel nicotinic agonist with subtype selectivity implicates the alpha4beta2* subtype in the modulation of dopamine release from rat striatal synaptosomes". The Journal of Neuroscience. 20 (8): 2783–91. doi:10.1523/JNEUROSCI.20-08-02783.2000. PMC 6772190. PMID 10751429.

[2] Cao YJ, Surowy CS, Puttfarcken PS (March 2005). "Nicotinic acetylcholine receptor-mediated [3H]dopamine release from hippocampus". The Journal of Pharmacology and Experimental Therapeutics. 312 (3): 1298–304. doi:10.1124/jpet.104.076794. PMID 15542623. S2CID 20437091.

[3] Gohlke H, Gündisch D, Schwarz S, Seitz G, Tilotta MC, Wegge T (February 2002). "Synthesis and nicotinic binding studies on enantiopure diazine analogues of the novel (2-chloro-5-pyridyl)-9-azabicyclo[4.2.1]non-2-ene UB-165". Journal of Medicinal Chemistry. 45 (5): 1064–72. doi:10.1021/jm010936y. PMID 11855986.

[4] Sharples CG, Karig G, Simpson GL, Spencer JA, Wright E, Millar NS, et al. (July 2002). "Synthesis and pharmacological characterization of novel analogues of the nicotinic acetylcholine receptor agonist (+/-)-UB-165". Journal of Medicinal Chemistry. 45 (15): 3235–45. doi:10.1021/jm020814l. PMID 12109907.

[5] Sutherland A, Gallagher T, Sharples CG, Wonnacott S (March 2003). "Synthesis of two fluoro analogues of the nicotinic acetylcholine receptor agonist UB-165". The Journal of Organic Chemistry. 68 (6): 2475–8. doi:10.1021/jo026698b. PMID 12636420.

[6] Karig G, Large JM, Sharples CG, Sutherland A, Gallagher T, Wonnacott S (September 2003). "Synthesis and nicotinic binding of novel phenyl derivatives of UB-165. Identifying factors associated with alpha7 selectivity". Bioorganic & Medicinal Chemistry Letters. 13 (17): 2825–8. doi:10.1016/S0960-894X(03)00594-8. PMID 14611837.

[1]

[2]

[3]

[4]

[5]

[6]

PROFILPELAJAR.COM

UB-165

References

Read other articles:

What Pet Should I Get?

David Brooks

Totok Sugiharto

Hotel Bellevue (Berlín)

Western Circus (Lucky Luke)

شادو أوف ذا نينجا

The Eurovision Museum

FN P90

Serbian Australians

Geography of Korea

Indestructible (Robyn song)

Roman Badanin

Matt Ishida

St. Paul College, Pasig

Necile

Москва в годы Великой Отечественной войны

Roman Catholic Archdiocese of Cuiabá

Norton, Kansas

Peski Kyzylkum (kamadan)

Sahale Arm