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Phytotoxic Effects and Phytochemical Fingerprinting of Hydrodistilled Oil, Enriched Fractions, and Isolated Compounds Obtained from Cryptocarya massoy (Oken) Kosterm. Bark

The hydrodistilled oil of Cryptocarya massoy bark was characterized by GC‐FID and GC/MS analyses, allowing the identification of unusual C10 massoia lactone (3, 56.2%), C12 massoia lactone (4, 16.5%), benzyl benzoate (1, 12.7%), C8 massoia lactone (3.4%), δ‐decalactone (5, 1.5%), and benzyl salicyla...

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Published in:Chemistry & biodiversity 2016-01, Vol.13 (1), p.66-76
Main Authors: Rolli, Enrico, Marieschi, Matteo, Maietti, Silvia, Guerrini, Alessandra, Grandini, Alessandro, Sacchetti, Gianni, Bruni, Renato
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description The hydrodistilled oil of Cryptocarya massoy bark was characterized by GC‐FID and GC/MS analyses, allowing the identification of unusual C10 massoia lactone (3, 56.2%), C12 massoia lactone (4, 16.5%), benzyl benzoate (1, 12.7%), C8 massoia lactone (3.4%), δ‐decalactone (5, 1.5%), and benzyl salicylate (2, 1.8%) as main constituents. The phytotoxic activities of the oil, three enriched fractions (lactone‐rich, ester‐rich, and sesquiterpene‐rich), and four constituents (compounds 1, 2, 5, and δ‐dodecalactone (6)) against Lycopersicon esculentum and Cucumis sativus seeds and seedlings were screened. At a concentration of 1000 μl/l, the essential oil and the massoia lactone‐rich fraction caused a complete inhibition of the germination of both seeds, and, when applied on tomato plantlets, they induced an 85 and 100% dieback, respectively. These performances exceeded those of the well‐known phytotoxic essential oils of Syzygium aromaticum and Cymbopogon citratus, already used in commercial products for the weed and pest management. The same substances were also evaluated against four phytopathogenic bacteria and ten phytopathogenic fungi, providing EC50 values against the most susceptible strains in the 100–500 μl/l range for the essential oil and in the 10–50 μl/l range for compound 6 and the lactone‐rich fraction. The phytotoxic behavior was related mainly to massoia lactones and benzyl esters, while a greater amount of 6 may infer a good activity against some phytopathogenic fungi. Further investigations of these secondary metabolites are warranted, to evaluate their use as natural herbicides.
doi_str_mv 10.1002/cbdv.201500010
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Bark</atitle><jtitle>Chemistry &amp; biodiversity</jtitle><addtitle>Chemistry &amp; Biodiversity</addtitle><date>2016-01</date><risdate>2016</risdate><volume>13</volume><issue>1</issue><spage>66</spage><epage>76</epage><pages>66-76</pages><issn>1612-1872</issn><eissn>1612-1880</eissn><abstract>The hydrodistilled oil of Cryptocarya massoy bark was characterized by GC‐FID and GC/MS analyses, allowing the identification of unusual C10 massoia lactone (3, 56.2%), C12 massoia lactone (4, 16.5%), benzyl benzoate (1, 12.7%), C8 massoia lactone (3.4%), δ‐decalactone (5, 1.5%), and benzyl salicylate (2, 1.8%) as main constituents. The phytotoxic activities of the oil, three enriched fractions (lactone‐rich, ester‐rich, and sesquiterpene‐rich), and four constituents (compounds 1, 2, 5, and δ‐dodecalactone (6)) against Lycopersicon esculentum and Cucumis sativus seeds and seedlings were screened. At a concentration of 1000 μl/l, the essential oil and the massoia lactone‐rich fraction caused a complete inhibition of the germination of both seeds, and, when applied on tomato plantlets, they induced an 85 and 100% dieback, respectively. These performances exceeded those of the well‐known phytotoxic essential oils of Syzygium aromaticum and Cymbopogon citratus, already used in commercial products for the weed and pest management. The same substances were also evaluated against four phytopathogenic bacteria and ten phytopathogenic fungi, providing EC50 values against the most susceptible strains in the 100–500 μl/l range for the essential oil and in the 10–50 μl/l range for compound 6 and the lactone‐rich fraction. The phytotoxic behavior was related mainly to massoia lactones and benzyl esters, while a greater amount of 6 may infer a good activity against some phytopathogenic fungi. Further investigations of these secondary metabolites are warranted, to evaluate their use as natural herbicides.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><pmid>26765353</pmid><doi>10.1002/cbdv.201500010</doi><tpages>11</tpages></addata></record>
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subjects Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - isolation & purification
Anti-Bacterial Agents - pharmacology
Anti-Bacterial Agents - toxicity
Antifungal Agents - chemistry
Antifungal Agents - isolation & purification
Antifungal Agents - pharmacology
Antifungal Agents - toxicity
Antimicrobial activity
Bacteria - drug effects
Cryptocarya
Cryptocarya - chemistry
Cryptocarya massoy
Cucumis sativus
Cucumis sativus - drug effects
Cucumis sativus - growth & development
Cymbopogon citratus
Dose-Response Relationship, Drug
Essential oil
Fungi - drug effects
Lycopersicon esculentum
Lycopersicon esculentum - drug effects
Lycopersicon esculentum - growth & development
Massoia lactones
Microbial Sensitivity Tests
Molecular Structure
Phytotoxicity
Plant Bark - chemistry
Plant Oils - chemistry
Plant Oils - isolation & purification
Plant Oils - pharmacology
Pyrones
Seeds - drug effects
Seeds - growth & development
Structure-Activity Relationship
Syzygium aromaticum
title Phytotoxic Effects and Phytochemical Fingerprinting of Hydrodistilled Oil, Enriched Fractions, and Isolated Compounds Obtained from Cryptocarya massoy (Oken) Kosterm. Bark
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