Louis Piovetti
University of Perpignan
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Louis Piovetti.
Journal of Natural Products | 2008
Redouane Mokrini; Mohammed Ben Mesaoud; Mohammed Daoudi; Claire Hellio; Jean-Philippe Maréchal; Mohamed El Hattab; Annick Ortalo-Magné; Louis Piovetti; Gérald Culioli
The brown alga Cystoseira baccata harvested along the Atlantic coasts of Morocco yielded seven new meroditerpenoids (1-4) and derivatives (5-7), whose chemical structures were elucidated mainly by 2D NMR and mass spectrometry. Surprisingly, for all these compounds, which possess a bicyclo[4.3.0]nonane ring system, a trans fusion of the bicyclic system was deduced by stereochemical studies even though such compounds isolated from Cystoseira species are known to have a typical cis orientation for the bridgehead methyls. The antifouling and antibacterial activities of compounds 1-5 and 7 were evaluated, as well as their toxicity toward nontarget species. Compounds 4, 5, and 7 showed antifouling activities against growth of microalgae, macroalgal settlement, and mussel phenoloxidase activity, while being nontoxic to larvae of sea urchins and oysters.
Journal of Natural Products | 2009
Yannick Viano; Dominique Bonhomme; Mercedes Camps; Jean-François Briand; Annick Ortalo-Magné; Yves Blache; Louis Piovetti; Gérald Culioli
Four new cyclized diterpenes, one xenicane (1) and three dolabellanes (2-4), were isolated, along with seven previously reported metabolites [3beta-hydroxydilophol (5), dictyols E (6) and C (7), hydroxycrenulide (8), 9-acetoxy-15-hydroxy-1,6-dollabelladiene (9), hydroxyacetyldictyolal (10), and fucoxanthin], from a Mediterranean species of Dictyota sp. collected in Le Brusc Lagoon (French Mediterranean coast). Their structures, as well as their relative configurations, were determined through extensive spectrometric (IR, HRESIMS, 1D and 2D NMR) data analysis and molecular modeling studies and by comparison with those reported in literature. Some of the isolated metabolites were evaluated for their antiadhesion activity against a marine bacterial biofilm (Pseudoalteromonas sp. D41).
Phytochemistry | 1983
Georges Combaut; Louis Piovetti
Abstract A novel epoxy-diterpene identified as 7,8-epoxy-1-hydroxy-13-keto-3,7,11,15-tetramethylhexadeca-2 E ,5 E ,10 E ,-14-tetraene was isolated from Bifurcaria bifurcata , a brown alga belonging to the family Cystoseiraceae, in which eleganolone, epoxy-eleganolone and eleganediol have previously been isolated.
Journal of Applied Phycology | 2006
Dimitri Moreau; Hélène Thomas-Guyon; Catherine Jacquot; Marcel Juge; Gérald Culioli; Annick Ortalo-Magné; Louis Piovetti; Christos Roussakis
In this study, the antiproliferative activity of a crude extract isolated from Bifurcaria bifurcata (Velley) Ross, a common marine brown alga of the Atlantic shores of Europe, was investigated. Its antiproliferative effect on asynchronous cells of a human non-small-cell bronchopulmonary carcinoma line (NSCLC-N6), particularly chemo-resistant, was expected in vitro. Cell growth appeared to be inhibited in the G1 phase of the cell cycle, and kinetic studies in pretreated cells showed that this growth arrest was irreversible. These events are related to a terminal differentiation induction.
Phytochemistry | 1981
Louis Piovetti; Christian Francisco; Ginette Pauly; Otmane Benchabane; Colette Bernard-Dagan; Anne Diara
Abstract Analysis of wood essential oil of Cupressus dupreziana revealed 26 components: 13 monoterpenes and 13 sesquiterpenes. The main components were carv
Phytochemistry | 1980
Louis Piovetti; Georges Combaut; Anne Diara
Resume Twelve oxygenated mono- and sesquiterpenes have been isolated from the heartwood extractives of Cupressus dupreziana. Six of them are new compounds with p-menthane, alaskane and 1,7-diepicedrane skeletons. Structures were determined by spectral methods. The chemotaxonomic significance of these findings are discussed.
Phytochemistry | 1977
Louis Piovetti; Anne Diara
Abstract Heartwood extractives of C. dupreziana were investigated. Carvacrol methyl ether, cedrol and α-cedrene are present, together with sesquiterpene hydrocarbons. A comparison is made with those found in C. sempervirens and other Cupressus species.
Phytochemistry | 1983
Ginette Pauly; Abdelhamid Yani; Louis Piovetti; Colette Bernard-Dagan
Abstract The essential oils of the leaves of Cupressus dupreziana and Cupressus sempervirens were compared. The composition of the hydrocarbon fraction showed a great similarity between the two species.
Journal of Chromatography A | 1983
Léon Serve; Louis Piovetti; Nicole Longuemard
Abstract Analysis of phenolic acids and aldehydes by high-performance liquid chromatography: a comparative analysis of high mountain soils and their vegetation. A method is described for the analysis of phenolic acids and aldehydes by reversed-phase high-performance liquid chromatography with a ternary isocratic elution system. It is applied to the separation and the estimation of phenolic compounds issued from: (1) pyrenean soils at high altitude (Pyrenees-Orientales, France, 2500 m), and (2) the main plant growing there. Phenolic extracts of soil and plant are isolated exactly in the same way by the procedure described.
Phytochemistry | 1980
Louis Piovetti; Emmanuel Gonzalez; Anne Diara
Abstract The heartwood of Cupressus dupreziana and C. sempervirens were shown to contain similar mixtures of diterpenes.