Ebalzotan
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| Routes of administration  | Oral | 
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IUPAC name 
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| Formula | C19H30N2O2 | 
| Molar mass | 318.461 g·mol−1 | 
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Ebalzotan (NAE-086) is a selective 5-HT1A receptor agonist.[1][2] It was under development as an antidepressant and anxiolytic agent but produced undesirable side effects in phase I clinical trials and was subsequently discontinued.[1][2]
See also
References
- 1 2 Braish T, Gadamasetti KG (2008). Process chemistry in the pharmaceutical industry, volume 2 challenges in an ever changing climate. Boca Raton: CRC Press. ISBN 978-0-8493-9051-7.
 - 1 2 Weaver DF, Nogrady T, Nogrady T (2005). Medicinal chemistry a molecular and biochemical approach. Oxford [Oxfordshire]: Oxford University Press. ISBN 0-19-510455-2.
 
| 5-HT1ARTooltip 5-HT1A receptor agonists | |
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| GABAARTooltip GABAA receptor PAMsTooltip positive allosteric modulators | 
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| Hypnotics | |
| Gabapentinoids (α2δ VDCC blockers)  | |
| Antidepressants | 
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| Antipsychotics | |
| Sympatholytics (Antiadrenergics)  | 
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| Others | |
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Serotonin receptor modulators  | |||||||||||||||||||||||||||||||||||||||
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| 5-HT1 | 
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| 5-HT2 | 
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| 5-HT3–7 | 
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