Ces travaux de thèse portent sur l’étude chimique d’espèces marines échantillonnées en Méditerranée. Dans le cadre du projet VALBIM, co-financé par la région PACA et en étroite collaboration avec la société BioPreserv à Grasse mais également avec la Mycoteca Universitatis Taurinensis (MUT) de l’Université de Turin, nous avons isolé et caractérisé 21 molécules dont 14 se sont avérées nouvelles. L’étude de l’algue Caulerpa taxifolia a conduit à la caulerpényne et à quatre nouveaux dérivés de l’acide pyruvique sulfatés. Les travaux sur l’ascidie Polysyncraton sp. ont conduit aux bolascidines A-D, quatre nouveaux métabolites de type bolaamphiphiles dont il n’existe pas à notre connaissance d’équivalent naturel ou synthétique. La première étude chimique de l’éponge Hexadella racovitzai a conduit à deux dérivés de la bromotyrosine, la psammapline A et une nouvelle molécule, la 4-Osulfatocyclobispsammapline A. Par ailleurs, trois nouvelles crambescines C1, conjointement avec une crambescine A2 déjà répertoriée, ont été isolées de Crambe crambe. L’étude du champignon marin Stachybotrys chartarum, isolé de l’éponge Aplysina cavernicola, a conduit à la satratoxine H et à deux nouveau dérivé, la 2,3-dihydrosatratoxine H et l’épi-chartarutine G, ainsi qu’à trois dérivés stachybotrylactame déjà répertoriés dans la bibliographie. Les différents métabolites ont été évalués pour leurs propriétés antibactériennes et cytotoxiques. Ces travaux ont bénéficié de nouvelles approches analytiques (calculs des spectres de dichroïsme circulaire électroniques par TDDFT, réseaux moléculaires) permettant de renforcer l’intérêt des études liées à l’écologie chimique et à la recherche de nouvelles molécules bioactives potentiellement valorisables dans différents domaines. / This PhD work focuses on the chemical study of marine species sampled in the Mediterranean Sea. As part of the VALBIM project, cofinanced by the region PACA and in close collaboration with the SME BioPreserv in Grasse but also with the Mycoteca Universitatis Taurinensis (MUT) of the University of Turin, we have isolated and characterized 21 molecules in total.14 of them were never reported before. The study of the seaweed Caulerpa taxifolia led to caulerpenyne and four new sulphated pyruvic acid derivatives. The work on the ascidian Polysyncraton sp. led to bolascidins A-D, four new metabolites which belong to the bolaamphiphile family, which, to the best of our knowledge, have no natural or synthetic equivalent. The first chemical study of the sponge Hexadella racovitzai led to two bromotyrosine derivatives, psammapline A and a new molecule, 4-O-sulfatocyclobispsammapline A. In addition, three new C1 crambescins, together with one crambescine A2 already reported, have been isolated from Crambe crambe. For all isolated marine invertebrate metabolites, the producer(s) remain(s) to be explored. The study of the marine fungus Stachybotrys chartarum, isolated from the sponge Aplysina cavernicola, led to satratoxin H and three stachybotrylactam derivatives already reported in the literature, and to 2,3-dihydrosatratoxin H and epi-chartarutine G, two new natural products. The different metabolites were evaluated for their antibacterial and cytotoxic properties. This work benefited from new analytical approaches (calculations of electronic circular dichroïsm spectra by TDDFT, molecular networking) and reinforced the interest of studies related to chemical ecology and search for new bioactive molecules to be valorized in different areas.

O presente projeto de pesquisa teve por objetivo a descoberta de metabólitos secundários potencialmente bioativos contra atividade parasitária e como agentes anti-virais e antibióticos, usando desreplicação como metodologia essencial na seleção e priorização de extratos brutos oriundos de invertebrados, para a descoberta de produtos naturais estruturalmente inéditos.<br /><br />Foram preparados diversos extratos de invertebrados marinhos a partir de um fracionamento inicial. O desenvolvimento e a aplicação de uma metodologia de desreplicação permitiu a seleção de três organismos de estudo, Iotrochota birotulata, Amathia verticillata, e Tedania brasiliensis. Os extratos destes organismos foram submetidos a diferentes metodologias de fracionamento, isolamento e purificação de substâncias, dependendo dos resultados de desreplicação para cada organismo.<br /><br />Como resultado do isolamento e identificação de substancias destes organismos, obteve-se dois compostos já conhecidos na literatura e dezesseis compostos inéditos, dos quais dois são derivados sintéticos. De todos os compostos isolados, a pseudoceratidina, as desbromopseudoceratidinas e as tedamidas A e B apresentaram um índice de seletividade de 243.1, 217.1 e 89.3 respectivamente para Leishmania (L.) infantum, e o composto N12-acetilpseudoceratidina de 23.2 para Trypanosoma cruzi, sendo estes resultados muito promissores para a utilização das estruturas destas moléculas como potenciais modelos para o desenvolvimento de fármacos. / This research project aimed at the discovery of potentially bioactive secondary metabolites against parasitic activity and as antiviral agents and antibiotics, using dereplication as an essential methodology in the selection and prioritization of crude extracts derived from invertebrates, to the discovery of natural products structurally unpublished.<br /><br />Various extracts of marine invertebrates from an initial fractionation were prepared. The development and application of a dereplication methodology allowed the selection of three study organisms, Iotrochota birotulata, Amathia verticillata, and Tedania brasiliensis. The extracts of these organisms were subjected to different methods of fractionation, isolation and purification of substances, depending on the results of dereplication for each organism.<br /><br /> As a result of the isolation and identification of substances of these organisms, it obtained two compounds already known in the literature and unpublished sixteen compounds, two of which are synthetic derivatives. In all isolated compounds, pseudoceratidina, the desbromopseudoceratidinas and tedamidas A and B showed an index of selectivity 243.1, 217.1 and 89.3 respectively for Leishmania (L.) infantum, and the compound N12-acetilpseudoceratidina 23.2 for Trypanosoma cruzi, which are very promising results for the use of these molecules as structures potential models for drug development.