Access to 3-spiroindolizines containing an isoindole ring through intra-molecular arylation of spiro-N-acyliminium species: a new family of potent farnesyltransferase inhibitors |
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Antagonists of the P2X7 receptor: mechanism of enantioselective recognition using highly sulfated and sulfobutylether cyclodextrins by capillary electrokinetic chromatography. |
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Antioxidant Activity of New Benzo[de]quinolines and Lactams: 2DQuantitative Structure-Activity Relationships |
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Bioantibio, molécules antibactériennes et antifongiques biosourcées. |
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Biosourced catalysts design : synthesis of organic molecules of interest from biosourced synthons and purification of contaminated matrices. |
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Conception, synthèse et évaluation pharmacologique d'inhibiteurs mixtes de la farnésyltransférase et de la polymérisation de la tubuline |
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Conformational Restriction Leading to a Selective CB2 Cannabinoid Receptor Agonist Orally Active Against Colitis. |
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Discovery of ferrocene-containing farnesyltransferase inhibitors. Investigation of bulky lipophilic groups for the A2 binding site of farnesyltransferase |
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Discovery of indolizines containing triazine moiety as new leads for the development of antitumoral agents targeting mitotic events. |
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Eaton's reagent-mediated domino π-cationic arylations of aromatic carboxylic acids to Iasi-red polymethoxylated polycyclic aromatic hydrocarbons: products with unprecedented biological activities as tubulin polymerization inhibitors. |
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Efficacy and modes of action of new plant defense simulators on the wheat-Zymoseptoria tritici pathosystem. |
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An efficient one-pot reaction for the synthesis of pyrazolones bearing a phenothiazine unit |
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Élaboration de N,S-acétals cycliques et leur transposition en 1,4-thiazines selon des processus en cascade : Nouveaux inhibiteurs de la farnésyltransférase |
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Enhanced antitumor potential induced by chloroacetate-loaded benzophenones acting as fused tubulin-pyruvate dehydrogenase kinase 1 (PDHK1) ligands |
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Evaluation and comparison of three different separation techniques for analysis of retroamide enantiomers and their biological evaluation against h-P2X7 receptor |
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Exploring isoxazoles and pyrrolidinones decorated with the 4,6-dimethoxy-1,3,5-triazine unit as human farnesyltransferase inhibitors |
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From Conventional Lewis Acids to Heterogeneous Montmorillonite K10, Eco-friendly Plant-based Catalysts used as Green Lewis Acids. |
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Impact of Functional Groups on the Copper-Initiated N-Arylation of 5-Functionalized Pyrrolidin-2-ones and Their Vinylogues |
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Involvement of the P2X7 purinergic receptor in inflammation: an update of antagonists series since 2009 and their promising therapeutic potential. |
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Methylene versus carbonyl bridge in the structure of new tubulin polymerization inhibitors with tricyclic A-rings. |
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New Efficient Eco-Friendly Supported Catalysts for the Synthesis of Amides with Antioxidant and Anti-Inflammatory Properties |
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New salicylic acid and pyroglutamic acid conjugated derivatives confer protection to bread wheat against Zymoseptoria tritici |
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On the discovery of new potent human farnesyltransferase inhibitors: emerging pyroglutamic derivatives. |
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P2X7R, an innovation for the treatment of inflammatory diseases and cancer : an innovation for the treatment of inflammatory diseases and cancer. |
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P2X7R, une innovation dans le traitement des maladies inflammatoires et du cancer |
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Performance comparison of chlorinated chiral stationary phases in supercritical fluid chromatography for separation of selected pyrrolidone derivatives |
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Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds. |
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Phenyliodine(III) Diacetate/I2 -Mediated Domino Approach for Pyrrolo[1,4]Thiazines and 1,4-Thiazines by a One-Pot Morin Rearrangement of N,S-Acetals |
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The potential of ryegrass (Lolium perenne L.) to clean up multi-contaminated soils from labile and phytoavailable potentially toxic elements to contribute into a circular economy |
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Pyroglutamide-Based P2X7 Receptor Antagonists Targeting Inflammatory Bowel Disease |
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The Reactivity of Enantiopure (S )-6-Oxopipecolic Acid and Corresponding Pyridoisoquinolines Under Acidic Conditions |
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The revisited synthesis of tert-butyl pyroglutamate derivatives |
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Separations of antifungal compounds in capillary electrophoresis with two anionic cyclodextrins |
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A Small Aromatic Compound Has Antifungal Properties and Potential Anti-Inflammatory Effects against Intestinal Inflammation |
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Studies on indolizines. Evaluation of their biological properties as microtubule-interacting agents and as melanoma targeting compounds. |
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Studies on Pyrrolidinones: Chemistry of Dimethoxytriazines |
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Studies on pyrrolidinones. On the application of copper-catalyzed arylation of methyl pyroglutamate to obtain a new benzo[de]quinoline scaffold |
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Studies on pyrrolidinones. Reaction of pyroglutamic acid and vinylogues with aromatics in Eaton’s reagent |
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Supercritical fluid chromatography approach for a sustainable manufacture of new stereoisomeric anticancer agent |
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A sustainable approach to manage metal-contaminated soils: a preliminary greenhouse study for the possible production of metal-enriched ryegrass biomass for biosourced catalysts |
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Synthesis and anticancer activity of analogues of phenstatin, with a phenothiazine A-ring, as a new class of microtubule-targeting agents |
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Synthesis and biological evaluation of phenstatin metabolites |
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Synthesis of metallo-B-lactamases inhibitors to fight the bacterial resistance to B-lactam antibiotics. |
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Synthesis of triazoloquinazolinone based compounds as tubulin polymerization inhibitors and vascular disrupting agents. |
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Toward a New Way for the Valorization of Miscanthus Biomass Produced on Metal-Contaminated Soils Part 1: Mesocosm and Field Experiments |
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Valorisation en synthèse organique d'éco-catalyseurs hétérogènes régénérables à partir de matériaux verts cultivés sur des sols contaminés |
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Valorization in organic synthesis of heterogeneous eco-catalysts produced from green materials grown on contaminated soils.. |
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