Phenylpropanoid conjugated iridoids with anti-malarial activity from the leaves of Morinda morindoides

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Abstract
Two phenylpropanoid-conjugated iridoids, deglucosyl gaertneroside (1) and morindoidin (2), were isolated from the leaves of Morinda morindoides (Rubiaceae) by activity-guided fractionation using an anti-malarial activity assay. The known related iridoids molucidin (3) and prismatomerin (4), two lignans, abscisic acid, two megastigmanes, and two flavonol glycosides were also identified. The structures of isolated compounds were elucidated using spectroscopic analysis. The isolated compounds were evaluated for anti-malarial activity against the chloroquine/mefloquine-sensitive strains of Plasmodium falciparum together with cytotoxicity against adult mouse brain cells. Potent anti-malarial activity of 3 and 4 (IC50 of 0.96 and 0.80 μM, CC50 of 1.02 and 0.88 μM, and SI of 1.06 and 1.10, respectively) was shown, while new iridoids 1 and 2 and pinoresinol (5) displayed moderate activity (IC50 of 40.9, 20.6, and 24.2 μM) without cytotoxicity (CC50 > 50 μM). These results indicate that 1–5 may be promising lead compounds for anti-malarial drugs. In addition, our results imply the necessity of the quality control of the extract of M. morindoides leaves based on the contents of 1–5 in terms of the safety and efficacy.
Funding Information
  • the Joint Usage/Research Center on Tropical Disease, Institute of Tropical Medicine, Nagasaki University (2016-Ippan-20, 2017-Ippan-16, 2018-Ippan-20, 2019-Ippan-22)
  • Grant-in-Aid for the Cooperative Research Project from Institute of Natural Medicine, University of Toyama
  • Kobayashi International Scholarship Foundation

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