Targeted Isolation of Monoterpene Indole Alkaloids from <i>Palicourea sessilis</i>

Phytochemical investigation of the alkaloid extract of <i>Palicourea sessilis</i> by LC-HRMS/MS using molecular networking and an in silico MS/MS fragmentation approach suggested the presence of several new monoterpene indole alkaloids. These compounds were isolated by semipreparative HPLC, and their structures confirmed by means of HRMS, NMR, and ECD measurements as 4-<i>N</i>-methyllyaloside (<b>3</b>), 4-<i>N</i>-methyl-3,4-dehydrostrictosidine (<b>4</b>), 4β-hydroxyisodolichantoside (<b>6</b>), and 4α-hydroxyisodolichantoside (<b>7</b>), as well as the known alkaloids alline (<b>1</b>), <i>N</i>-methyltryptamine (<b>2</b>), isodolichantoside (<b>5</b>), and 5-oxodolichantoside (<b>8</b>). In addition, the acetylcholinesterase inhibitory activity of the compounds was evaluated up to 50 μM

Targeted Isolation of Monoterpene Indole Alkaloids from <i>Palicourea sessilis</i>

Phytochemical investigation of the alkaloid extract of <i>Palicourea sessilis</i> by LC-HRMS/MS using molecular networking and an in silico MS/MS fragmentation approach suggested the presence of several new monoterpene indole alkaloids. These compounds were isolated by semipreparative HPLC, and their structures confirmed by means of HRMS, NMR, and ECD measurements as 4-<i>N</i>-methyllyaloside (<b>3</b>), 4-<i>N</i>-methyl-3,4-dehydrostrictosidine (<b>4</b>), 4β-hydroxyisodolichantoside (<b>6</b>), and 4α-hydroxyisodolichantoside (<b>7</b>), as well as the known alkaloids alline (<b>1</b>), <i>N</i>-methyltryptamine (<b>2</b>), isodolichantoside (<b>5</b>), and 5-oxodolichantoside (<b>8</b>). In addition, the acetylcholinesterase inhibitory activity of the compounds was evaluated up to 50 μM