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Bioactive Constituents of Juniperus turbinata Guss . from La Maddalena Archipelago
Author(s) -
Venditti Alessandro,
Maggi Filippo,
Quassinti Luana,
Bramucci Massimo,
Lupidi Giulio,
Ornano Luigi,
Ballero Mauro,
Sanna Cinzia,
Bruno Maurizio,
Rosselli Sergio,
Bianco Armandodoriano
Publication year - 2018
Publication title -
chemistry and biodiversity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 70
eISSN - 1612-1880
pISSN - 1612-1872
DOI - 10.1002/cbdv.201800148
Subject(s) - chemistry , cupressaceae , amentoflavone , abts , dpph , monoterpene , phytochemical , chemotype , essential oil , trolox , linalool , botany , traditional medicine , antioxidant , food science , biochemistry , biology , medicine , pollen
A comprehensive phytochemical study of Juniperus turbinata (Cupressaceae) collected from La Maddalena Archipelago (Sardinia, Italy) is reported. Both the essential oil and the ethanolic extract obtained from the aerial parts were analyzed. The essential oil appears to belong to a new chemotype compared to other Mediterranean juniper accessions, as it was favored by geographic isolation of the isles. It showed a low content of monoterpene hydrocarbons and α ‐terpineol, ent ‐manoyl oxide, 1,10‐di‐ epi ‐cubenol as the major constituents. The ethanolic fraction contained mainly diterpenoids. Among these, 15‐formyloxyimbricatolic acid ( 7 ) is a new natural product since it has hitherto been obtained only by synthetic route. The phenolic fraction contained biflavonoids: cupressuflavone ( 9 ), followed by minor amounts of amentoflavone ( 10 ) and hinokiflavone ( 11 ). The essential oil and six purified compounds ( 1 – 4 , 8 and 9 ) were assessed for biological activities, namely antioxidant (assessed by DPPH · , ABTS ·+ and FRAP methods) and cytotoxic effects towards selected human tumor cell lines ( MDA ‐ MB 231, A375 and HCT 116 cells). Compound 3 exhibited higher radical scavenging activity against ABTS ·+ radical than the reference Trolox. Noteworthy, compound 8 showed powerful effects towards tumor cell lines, with IC 50 values in the range of 0.060 – 0.201 μ m , which make it a promising anticancer drug candidate.