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Trichilianones A-D, Novel Cyclopropane-Type Limonoids from Trichilia adolfi.


ABSTRACT: The fractionation of an ethanol extract of the bark of Trichilia adolfi yielded four novel limonoids (trichilinones A-D, 1-4), with five fused rings and related to the hortiolide-type limonoids. Starting with an ?-lactone, which is ?,?-unsaturated in trichilinones A and D (1 and 4), attached to a tetrahydrofuran ring that is connected to an unusual bicyclo [5.1.0] hexane system, joined with a cyclopentanone with a 3-furanyl substituent [(2-oxo)-furan-(5H)-3-yl in trichilinone D (4)], the four compounds isolated display a new 7/5/3/5/5 limonoid ring system. Their structures were established based on extensive analysis of NMR spectroscopic data. As the crude extract possessed anti-leishmanial properties, the compounds were assayed for cytotoxic and anti-parasitic activities in vitro in murine macrophages cells (Raw 264.7) and leishmania promastigotes (L. amazoniensis and L. braziliensis), respectively. The compounds showed moderate cytotoxicity (approximately 70 ?g/mL), but are not responsible for the leishmanicidal effect of the extract.

SUBMITTER: Limachi I 

PROVIDER: S-EPMC7919047 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

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Trichilianones A-D, Novel Cyclopropane-Type Limonoids from <i>Trichilia adolfi</i>.

Limachi Ivan I   Gonzalez-Ramirez Mariela M   Manner Sophie S   Ticona Juan C JC   Salamanca Efrain E   Gimenez Alberto A   Sterner Olov O  

Molecules (Basel, Switzerland) 20210215 4


The fractionation of an ethanol extract of the bark of <i>Trichilia adolfi</i> yielded four novel limonoids (trichilinones A-D, <b>1</b>-<b>4</b>), with five fused rings and related to the hortiolide-type limonoids. Starting with an ε-lactone, which is α,β-unsaturated in trichilinones A and D (<b>1</b> and <b>4</b>), attached to a tetrahydrofuran ring that is connected to an unusual bicyclo [5.1.0] hexane system, joined with a cyclopentanone with a 3-furanyl substituent [(2-oxo)-furan-(5<i>H</i>  ...[more]

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