Chemistry:Liafensine
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Short description: Chemical compound
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Routes of administration | Oral |
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Formula | C24H22N4 |
Molar mass | 366.468 g·mol−1 |
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Liafensine (BMS-820836) is a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI) which was under development by Bristol-Myers Squibb for the treatment of major depressive disorder.[1][2] Though it demonstrated comparable effectiveness to escitalopram and duloxetine in phase II clinical trials, development was paused in 2013 because liafensine failed to show superior effectiveness relative to these drugs, a decision that was made likely based on its increased capacity for side effects as well as potential for abuse.[1] Another clinical trial of liafensine began in 2022.[3]
See also
References
- ↑ 1.0 1.1 "Digest". Progress in Neurology and Psychiatry 17 (5): 41–43. 2013. doi:10.1002/pnp.305. ISSN 1367-7543.
- ↑ "New Trends in Antidepressant Drug Research". Transporters as drug targets. Methods and Principles in Medicinal Chemistry. Weinheim, Germany: John Wiley & Sons. 2017. pp. 21–52 (22). doi:10.1002/9783527679430.ch2. ISBN 978-3-527-33384-4. https://books.google.com/books?id=uRauDQAAQBAJ&dq=Liafensine&pg=PA35.
- ↑ "CTG Labs - NCBI". https://clinicaltrials.gov/study/NCT05113771?start=2019-11-03_&aggFilters=funderType:industry,phase:2%203&limit=100&cond=depression&rank=74.
Original source: https://en.wikipedia.org/wiki/Liafensine.
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