期刊
JOURNAL OF NATURAL PRODUCTS
卷 -, 期 -, 页码 -出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.3c00443
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Three new bis-formyl phloroglucinol-meroterpenoids (1-3), three new euglobal type formylphloroglucinol-meroterpenoids (4-6), and one new dimeric formylphloroglucinol (7) were isolated from Eucalyptus camaldulensis leaves. Camaldulensal A (1) is the first bis-isovaleryl-formyl-phloroglucinol-sesquiterpenoid with a unique fused ring system and six stereogenic centers. Camaldulensals B (2) and C (3) are the first bis-isovaleryl-formyl-phloroglucinols conjugated to a monoterpene. The compounds showed significant antibacterial activity against methicillin-susceptible and methicillin-resistant Staphylococcus aureus strains.
Threenew bis-formyl phloroglucinol-meroterpenoids(1-3), three new euglobal type formylphloroglucinol-meroterpenoids(4-6), and one new dimeric formylphloroglucinol (7) were isolated from the leaves of Eucalyptus camaldulensis. Camaldulensal A (1) is the first bis-isovaleryl-formyl-phloroglucinol-sesquiterpenoid.It features a novel 6/6/10/3/6/6 fused ring system and contains sixstereogenic centers. Camaldulensals B (2) and C (3) are the first bis-isovaleryl-formyl-phloroglucinols, eachconjugated to a monoterpene. Formyl phloroglucinol compounds (FPCs)containing two spatially separated formyl phloroglucinols conjugatedto a terpene core such as 1-3 havenot been reported previously. The structures of these compounds wereelucidated by spectroscopic methods and computational analysis. CamaldulensalsB (2) and C (3) exhibited significant antibacterialactivity against methicillin-susceptible and methicillin-resistant Staphylococcus aureus. Structure activity relationshipsare discussed in relation to previously reported antibacterial activitiesof other molecules from the FPC structure class.
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