Leucettines, a Class of Potent Inhibitors of cdc2-Like Kinases and Dual Specificity, Tyrosine Phosphorylation Regulated Kinases Derived from the Marine Sponge Leucettamine B: Modul... von Debdab, Mansour, Carreaux, François, Renault, Steven, Soundararajan, Meera, Fedorov, Oleg, Filippakopoulos, Panagis, Lozach, Olivier, Babault, Lucie, Tahtouh, Tania, Baratte, Blandine, Ogawa, Yasushi, Hagiwara, Masatoshi, Eisenreich, Andreas, Rauch, Ursula, Knapp, Stefan, Meijer, Laurent, Bazureau, Jean-Pierre

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New Fusarochromanone Derivatives from the Marine Fungus Fusarium equiseti UBOCC-A-117302 von Pham, Giang Nam, Josselin, Béatrice, Cousseau, Arnaud, Baratte, Blandine, Dayras, Marie, Le Meur, Christophe, Debaets, Stella, Weill, Amélie, Robert, Thomas, Burgaud, Gaëtan, Probert, Ian, Abdoul-Latif, Fatouma Mohamed, Boyer, Laurent, Bach, Stéphane, Mehiri, Mohamed

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Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor von Ahmadu, Augustine A., Delehouze, Claire, Haruna, Anas, Mustapha, Lukman, Lawal, Bilqis A., Udobre, Aniefiok, Baratte, Blandine, Triscornia, Camilla, Autret, Axelle, Robert, Thomas, Bulinski, Jeannette Chloe, Rousselot, Morgane, Eugenio, Melanie Simoes, Dimanche-Boitrel, Marie-Therese, Petzer, Jacobus P., Legoabe, Lesetja J., Bach, Stephane

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Structure Activity Relationship Studies around DB18, a Potent and Selective Inhibitor of CLK Kinases von Brahmaiah, Dabbugoddu, Bhavani, Anagani Kanaka Durga, Aparna, Pasula, Kumar, Nangunoori Sampath, Solhi, Hélène, Le Guevel, Rémy, Baratte, Blandine, Robert, Thomas, Ruchaud, Sandrine, Bach, Stéphane, Jadav, Surender Singh, Reddy, Chada Raji, Mosset, Paul, Gouault, Nicolas, Levoin, Nicolas, Grée, René

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Dibenzofuran Derivatives Inspired from Cercosporamide as Dual Inhibitors of Pim and CLK1 Kinases von Viet Hung Dao, Ourliac-Garnier, Isabelle, Loge, Cedric, McCarthy, Florence O., Bach, Stephane, da Silva, Teresinha Goncalves, Denevault-Sabourin, Caroline, Thiefaine, Jerome, Baratte, Blandine, Robert, Thomas, Gouilleux, Fabrice, Brachet-Botineau, Marie, Bazin, Marc-Antoine, Marchand, Pascal

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Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi von Nguyen, Thi-Ngoc-Dung, Feizbakhsh, Omid, Sfecci, Estelle, Baratte, Blandine, Delehouzé, Claire, Garcia, Adrien, Moulin, Corentin, Colas, Pierre, Ruchaud, Sandrine, Mehiri, Mohamed, Bach, Stéphane

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Design of new disubstituted imidazo[1,2-b]pyridazine derivatives as selective Haspin inhibitors. Synthesis, binding mode and anticancer biological evaluation von Elie, Jonathan, Feizbakhsh, Omid, Desban, Nathalie, Josselin, Béatrice, Baratte, Blandine, Bescond, Amandine, Duez, Julien, Fant, Xavier, Bach, Stéphane, Marie, Dominique, Place, Matthieu, Ben Salah, Sami, Chartier, Agnes, Berteina-Raboin, Sabine, Chaikuad, Apirat, Knapp, Stefan, Carles, Fabrice, Bonnet, Pascal, Buron, Frédéric, Routier, Sylvain, Ruchaud, Sandrine

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Anti-mitotic properties of indirubin-3'-monoxime, a CDK/GSK-3 inhibitor: induction of endoreplication following prophase arrest von DAMIENS, Eve, BARATTE, Blandine, MARIE, Dominique, EISENBRAND, Gerhard, MEIJER, Laurent

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Synthesis, antileishmanial activity and cytotoxicity of 2,3-diaryl- and 2,3,8-trisubstituted imidazo[1,2-a]pyrazines von Marchand, Pascal, Bazin, Marc-Antoine, Pagniez, Fabrice, Rivière, Guillaume, Bodero, Lizeth, Marhadour, Sophie, Nourrisson, Marie-Renée, Picot, Carine, Ruchaud, Sandrine, Bach, Stéphane, Baratte, Blandine, Sauvain, Michel, Pareja, Denis Castillo, Vaisberg, Abraham J., Le Pape, Patrice

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From Quinoxaline, Pyrido[2,3- b ]pyrazine and Pyrido[3,4- b ]pyrazine to Pyrazino-Fused Carbazoles and Carbolines von Lassagne, Frédéric, Langlais, Timothy, Caytan, Elsa, Limanton, Emmanuelle, Paquin, Ludovic, Boullard, Manon, Courtel, Coline, Curbet, Idriss, Gédéon, Clément, Lebreton, Julien, Picot, Laurent, Thiéry, Valérie, Souab, Mohamed, Baratte, Blandine, Ruchaud, Sandrine, Bach, Stéphane, Roisnel, Thierry, Mongin, Florence

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Bioactive Metabolites from the Deep Subseafloor Fungus Oidiodendron griseum UBOCC-A-114129 von Navarri, Marion, Jégou, Camille, Bondon, Arnaud, Pottier, Sandrine, Bach, Stéphane, Baratte, Blandine, Ruchaud, Sandrine, Barbier, Georges, Burgaud, Gaëtan, Fleury, Yannick

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Neurymenolide A, a Novel Mitotic Spindle Poison from the New Caledonian Rhodophyta Phacelocarpus neurymenioides von Motuhi, Sofia-Eléna, Feizbakhsh, Omid, Foll-Josselin, Béatrice, Baratte, Blandine, Delehouzé, Claire, Cousseau, Arnaud, Fant, Xavier, Bulinski, Jeannette Chloë, Payri, Claude Elisabeth, Ruchaud, Sandrine, Mehiri, Mohamed, Bach, Stéphane

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Synthesis and biological studies of new quinazolines with ether functions in position 2 von Brahmaiah, Dabbugoddu, Bhavani, Anagani Kanaka Durga, Aparna, Pasula, Kumar, Nangunoori Sampath, Solhi, Hélène, Guevel, Rémy Le, Baratte, Blandine, Ruchaud, Sandrine, Bach, Stéphane, Mosset, Paul, Grée, René

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Synthetic Development of New 3-(4-Arylmethylamino)butyl-5-arylidene-rhodanines under Microwave Irradiation and Their Effects on Tumor Cell Lines and against Protein Kinases von Dago, Camille Déliko, Ambeu, Christelle N'ta, Coulibaly, Wacothon-Karime, Békro, Yves-Alain, Mamyrbékova, Janat, Defontaine, Audrey, Baratte, Blandine, Bach, Stéphane, Ruchaud, Sandrine, Guével, Rémy Le, Ravache, Myriam, Corlu, Anne, Bazureau, Jean-Pierre

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Synthesis and biological evaluation of Haspin inhibitors: Kinase inhibitory potency and cellular activity von Zeinyeh, Wael, Esvan, Yannick J., Josselin, Béatrice, Defois, Mathilde, Baratte, Blandine, Knapp, Stefan, Chaikuad, Apirat, Anizon, Fabrice, Giraud, Francis, Ruchaud, Sandrine, Moreau, Pascale

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Novel Thiazole-Fused [4,5-g] or [5,4-g]Quinazolin-8-ones and Their Quinazoline Analogues: Synthesis and Biological Evaluation von Broudic, Nathan, Pacheco-Benichou, Alexandra, Corbière, Cécile, Baratte, Blandine, Robert, Thomas, Bach, Stéphane, Solhi, Hélène, Le Guével, Rémy, Fruit, Corinne, Besson, Thierry

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New pyrido[3,4-g]quinazoline derivatives as CLK1 and DYRK1A inhibitors: synthesis, biological evaluation and binding mode analysis von Tazarki, Helmi, Zeinyeh, Wael, Esvan, Yannick J., Knapp, Stefan, Chatterjee, Deep, Schröder, Martin, Joerger, Andreas C., Khiari, Jameleddine, Josselin, Béatrice, Baratte, Blandine, Bach, Stéphane, Ruchaud, Sandrine, Anizon, Fabrice, Giraud, Francis, Moreau, Pascale

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Exploration of 7-azaindole-coumaranone hybrids and their analogues as protein kinase inhibitors von Qhobosheane, Malikotsi A., Beteck, Richard M., Baratte, Blandine, Robert, Thomas, Ruchaud, Sandrine, Bach, Stéphane, Legoabe, Lesetja J.

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Structure Activity Relationship Studies around IDB18/I, a Potent and Selective Inhibitor of CLK Kinases von Brahmaiah, Dabbugoddu, Bhavani, Anagani Kanaka Durga, Aparna, Pasula, Kumar, Nangunoori Sampath, Solhi, Hélène, Le Guevel, Rémy, Baratte, Blandine, Robert, Thomas, Ruchaud, Sandrine, Bach, Stéphane, Jadav, Surender Singh, Reddy, Chada Raji, Mosset, Paul, Gouault, Nicolas, Levoin, Nicolas, Grée, René

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From Synthetic Simplified Marine Metabolite Analogues to New Selective Allosteric Inhibitor of Aurora B Kinase von Juillet, Charlotte, Ermolenko, Ludmila, Boyarskaya, Dina, Baratte, Blandine, Josselin, Béatrice, Nedev, Hristo, Bach, Stéphane, Iorga, Bogdan I, Bignon, Jérôme, Ruchaud, Sandrine, Al-Mourabit, Ali

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