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Bradanicline

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Bradanicline
Clinical data
Other namesTC-5619
Identifiers
  • N-[(2S,3R)-2-(Pyridin-3-ylmethyl)-1-azabicyclo[2.2.2]oct-3-yl]-1-benzofuran-2- carboxamide
CAS Number
PubChemCID
IUPHAR/BPS
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC22H23N3O2
Molar mass361.445 g·mol−1
3D model (JSmol)
  • C1CN2CCC1[C@@H]([C@@H]2CC3=CN=CC=C3)NC(=O)C4=CC5=CC=CC=C5O4
  • InChI=1S/C22H23N3O2/c26-22(20-13-17-5-1-2-6-19(17)27-20)24-21-16-7-10-25(11-8-16)18(21)12-15-4-3-9-23-14-15/h1-6,9,13-14,16,18,21H,7-8,10-12H2,(H,24,26)/t18-,21-/m0/s1
  • Key:OXKRFEWMSWPKKV-RXVVDRJESA-N
  (verify)

Bradanicline (INN;[1] development codeTC-5619) is a drug which was beingdeveloped byTargacept that acts as apartial agonist at theα7 subtype of the neuralnicotinic acetylcholine receptors. It showed cognitive enhancing effects in animal studies, and was being developed through a collaboration between Targacept andAstraZeneca as a potential treatment forschizophrenia andattention deficit disorder.[2] Phase Iclinical trials were completed successfully, and it was in phase II trials.[3]

In May 2011,AstraZeneca declined to exercise its right to license the compound.[4] In September 2012, Targacept ended its development of badanicline for the purpose of treating ADHD in adults.[5] It was being studied for cognitive and memory enhancement.[6]

Bradanicline was discontinued forAlzheimer's disease and cognitive impairment in schizophrenia in late-2013.[7] It was also discontinued for ADHD.[7]

References

[edit]
  1. ^"International Nonproprietary Names for Pharmaceutical Substances (INN). Recommended International Nonproprietary Names: List 73"(PDF). World Health Organization. pp. 68–9. Retrieved3 January 2017.
  2. ^"TC-5619 Cognitive Dysfunction in Schizophrenia".Catalyst Biosciences. Archived fromthe original on August 20, 2008.
  3. ^Drahl C (September 2008)."Rethinking Schizophrenia".Chemical & Engineering News.86 (37):38–40.doi:10.1021/cen-v086n037.p038.
  4. ^"Targacept retains full development rights for TC-5619".Fierce Biotech. 2 May 2011.
  5. ^"Targacept ends development of ADHD drug".Market Watch. 17 September 2012.
  6. ^"Statement on a Nonproprietary Name Adopted by the USAN Council"(PDF). November 27, 2013.
  7. ^ab"Bradanicline - Attenua".AdisInsight. Springer Nature Switzerland AG.
Adamantanes
Adenosine antagonists
Alkylamines
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nAChRsTooltip Nicotinic acetylcholine receptors
Agonists
(andPAMsTooltip positive allosteric modulators)
Antagonists
(andNAMsTooltip negative allosteric modulators)
Precursors
(andprodrugs)
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