Abstract

Three new formyl phloroglucinol meroterpenoids, eumaidials A-C (1–3), were isolated from the leaves of Eucalyptus globulus subsp. maidenii, along with ten known analogues (4–13). Their chemical structures were determined by various spectral data and electronic circular dichroism calculations. Eumaidial A (1) is the first β-caryophyllene-based formyl phloroglucinol meroterpenoids from the genus Eucalyptus. Compounds 1–4 and 10 exhibited ATP-citrate lyase inhibitory activities, and compounds 2 and 3 suppressed the hepatocyte lipogenesis.

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