J
Ju-Yun Liu
Researcher at National Taiwan University
Publications - 9
Citations - 1114
Ju-Yun Liu is an academic researcher from National Taiwan University. The author has contributed to research in topics: Cinnamomum osmophloeum & Essential oil. The author has an hindex of 7, co-authored 7 publications receiving 1010 citations. Previous affiliations of Ju-Yun Liu include National Yang-Ming University.
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Journal ArticleDOI
Chemical Composition and Mosquito Larvicidal Activity of Essential Oils from Leaves of Different Cinnamomum osmophloeum Provenances
TL;DR: Results of larvicidal tests demonstrated that the leaf essential oils of cinnamaldehyde type and cinnAMaldehyde/cinnamyl acetate type had an excellent inhibitory effect against the fourth-instar larvae of Aedes aegypti.
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Study on the antiinflammatory activity of essential oil from leaves of Cinnamomum osmophloeum.
TL;DR: This study is the first to report antiinflammatory activity of extracts obtained from the leaf essential oil of C. osmophloeum, suggesting that essential oil was bioactive in antiinflammation in vitro.
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Chemical polymorphism and antifungal activity of essential oils from leaves of different provenances of indigenous cinnamon (Cinnamomum osmophloeum)
TL;DR: Results from the antifungal tests demonstrated that the leaf essential oils of cinnamaldehyde type and cinnAMaldehyde/cinnamyl acetate type had an excellent inhibitory effect against white-rot fungi, Trametes versicolor and Lenzites betulina and brown-rot fungus Laetiporus sulphureus.
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Insecticidal activities of leaf essential oils from Cinnamomum osmophloeum against three mosquito species.
TL;DR: Comparisons of mosquito larvicidal activity of trans-cinnamaldehyde congeners revealed that alpha-methyl cinnAMaldehyde, benzaldehyde, and trans- cinn amaldehyde exhibited strong mosquito larVicidal activity.
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Antifungal activity of cinnamaldehyde and eugenol congeners against wood-rot fungi
TL;DR: Results derived from the chemical structure-antifungal activity relationship study suggested that compounds with an aldehyde group or an acid group, a conjugated double bond and a length of CH chain outside the ring affect their antifungAL properties.