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Synthesis of Clausenamide Isomers and Evaluation of Their Potential as Cortical Neuroplastogens.

Yongyu Ou, Yara A Khatib, Adam Mosswood, Tarun K Roy, David A Gutierrez, David E. Olson, Jared T Shaw

ACS Chemical Neuroscience May 20, 2026 DOI: 10.1021/acschemneuro.5c00767 (opens in new tab)

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AI-extracted from the abstract
Characteristics Theoretical or philosophical paper Peer reviewed
Population Primary cortical cultures
Interventions Clausenamide stereoisomers (-)-cis-clausenamide
Measures high-content imaging
Keywords 5-ht2a partial agonist Clausenamide Multi-component reaction Neuroplastogen Psychoplastogen Synaptogenesis
Key points A one-pot, three-component synthesis provided six clausenamide stereoisomers and one analog, which showed a range of synaptogenic activities in primary cortical cultures. Postsynaptic effects of active compounds generally exceeded presynaptic effects, and (-)-cis-clausenamide produced the highest cortical synaptogenesis, an effect the authors suggest likely depends on its ability to act as a 5-HT2A receptor partial agonist.

Abstract

Neuroplastogens, small molecules that induce beneficial neuronal growth and plasticity, are a class of compounds emerging as new drugs for treating a range of central nervous system conditions. Clausenamide is a plasticity-promoting natural product isolated from the leaves of Clausena lansium, an evergreen native to Southeast Asia and southern China. Herein, we report an efficient synthesis of this compound by a one-pot, three-component assembly of three of the four contiguous stereogenic centers. This method enabled efficient access to six stereoisomers and one analog, which were evaluated for their ability to induce synaptogenesis in primary cortical cultures using high-content imaging. We observed a range of activities for clausenamide stereoisomers, but in general, the postsynaptic effects of the active compounds were greater than their presynaptic effects. Of the stereoisomers tested, (-)-cis-clausenamide exhibited the highest level of cortical synaptogenesis, with this effect likely being dependent on its ability to act as a 5-HT2AR partial agonist.

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