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Royal Society of Chemistry, MedChemComm, 3(9), p. 576-582

DOI: 10.1039/c7md00629b

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Synthesis and evaluation of nuciferine and roemerine enantiomers as 5-HT2 and α1 receptor antagonists

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

(R)-roemerine was found to be a potent 5-HT2A/C receptor antagonist with good selectivity compared to 5-HT2B and α1 receptor subtypes.