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Spongian Diterpenoids Derived from the Antarctic Sponge Dendrilla antarctica Are Potent Inhibitors of the Leishmania Parasite.


ABSTRACT: From the CH2Cl2 extract of the Antarctic sponge Dendrilla antarctica we found spongian diterpenes, including previously reported aplysulphurin (1), tetrahydroaplysulphurin-1 (2), membranolide (3), and darwinolide (4), utilizing a CH2Cl2/MeOH extraction scheme. However, the extracts also yielded diterpenes bearing one or more methyl acetal functionalities (5-9), two of which are previously unreported, while others are revised here. Further investigation of diterpene reactivity led to additional new metabolites (10-12), which identified them as well as the methyl acetals as artifacts from methanolysis of aplysulphurin. The bioactivity of the methanolysis products, membranoids A-H (5-12), as well as natural products 1-4, were assessed for activity against Leishmania donovani-infected J774A.1 macrophages, revealing insights into their structure/activity relationships. Four diterpenes, tetrahydroaplysulphurin-1 (2) as well as membranoids B (6), D (8), and G (11), displayed low micromolar activity against L. donovani with no discernible cytotoxicity against uninfected J774A.1 cells. Leishmaniasis is a neglected tropical disease that affects one million people every year and can be fatal if left untreated.

SUBMITTER: Shilling AJ 

PROVIDER: S-EPMC8351534 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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Spongian Diterpenoids Derived from the Antarctic Sponge <i>Dendrilla antarctica</i> Are Potent Inhibitors of the <i>Leishmania</i> Parasite.

Shilling Andrew J AJ   Witowski Christopher G CG   Maschek J Alan JA   Azhari Ala A   Vesely Brian A BA   Kyle Dennis E DE   Amsler Charles D CD   McClintock James B JB   Baker Bill J BJ  

Journal of natural products 20200413 5


From the CH<sub>2</sub>Cl<sub>2</sub> extract of the Antarctic sponge <i>Dendrilla antarctica</i> we found spongian diterpenes, including previously reported aplysulphurin (<b>1</b>), tetrahydroaplysulphurin-1 (<b>2</b>), membranolide (<b>3</b>), and darwinolide (<b>4</b>), utilizing a CH<sub>2</sub>Cl<sub>2</sub>/MeOH extraction scheme. However, the extracts also yielded diterpenes bearing one or more methyl acetal functionalities (<b>5</b>-<b>9</b>), two of which are previously unreported, whi  ...[more]

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