Bioassay-guided fractionation of the organic extract obtained from stem barks of the African plant Lophira lanceolata has led to the isolation of seven biflavonoids, including the new α’-chlorolophirone E (5) and 5’-chlorolophirone D (6). Among the isolated compounds, the bichalcone lophirone E was identified as a potent gametocytocidal agent with an IC50 value in the nanomolar range and negligible cytotoxicity (selectivity index = 570). Lophirone E proved to be about 100 times more active against P. falciparum stage V gametocytes than on asexual blood stages, thus exhibiting a unique stage-specific activity profile. The isolation of structural analogues allowed to draw preliminary structure-activity relationships, identifying the critical positions on the chemical scaffold of lophirone E.
Identification of a potent and selective gametocytocidal antimalarial agent from the stem barks of Lophira lanceolata / Lopatriello, Annalisa; Soré, Harouna; Habluetzel, Annette; Parapini, Silvia; D'Alessandro, Sarah; Taramelli, Donatella; Taglialatela-Scafati, Orazio. - In: BIOORGANIC CHEMISTRY. - ISSN 0045-2068. - 93:(2019), p. 103321. [10.1016/j.bioorg.2019.103321]
Identification of a potent and selective gametocytocidal antimalarial agent from the stem barks of Lophira lanceolata
Lopatriello, AnnalisaMembro del Collaboration Group
;Taglialatela-Scafati, Orazio
2019
Abstract
Bioassay-guided fractionation of the organic extract obtained from stem barks of the African plant Lophira lanceolata has led to the isolation of seven biflavonoids, including the new α’-chlorolophirone E (5) and 5’-chlorolophirone D (6). Among the isolated compounds, the bichalcone lophirone E was identified as a potent gametocytocidal agent with an IC50 value in the nanomolar range and negligible cytotoxicity (selectivity index = 570). Lophirone E proved to be about 100 times more active against P. falciparum stage V gametocytes than on asexual blood stages, thus exhibiting a unique stage-specific activity profile. The isolation of structural analogues allowed to draw preliminary structure-activity relationships, identifying the critical positions on the chemical scaffold of lophirone E.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.