alexa (+ -)-Nantenine analogs as antagonists at human 5-HT(2A) receptors: C1 and flexible congeners.
Chemistry

Chemistry

Medicinal Chemistry

Author(s): Chaudhary S, Pecic S, Legendre O, Navarro HA, Harding WW

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Abstract C1 and flexible analogs of (+/-)-nantenine were synthesized and evaluated for antagonist activity at human 5-HT(2A) receptors in a calcium mobilization assay. This work has resulted in the identification of the most potent 5-HT(2A) antagonist known based on an aporphine. Our results also suggest that the C1 position may be a key site for increasing 5-HT(2A) antagonist activity in this compound series. In addition, the structural rigidity of the aporphine core appears to be required for nantenine to function as a 5-HT(2A) antagonist.
This article was published in Bioorg Med Chem Lett and referenced in Medicinal Chemistry

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