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المؤلفون: Mohamed Benchekroun, Saoussen Oueslati, Sandrine Ventre, Kamsana Vijayakumar, Eddy Elisée, Laetitia A. Nguyen, Edithe Selwa, Robert H. Dodd, Linda Tlili, Alain Pruvost, Pascal Retailleau, Thierry Naas, Agustin Zavala, Bogdan I. Iorga, Agathe C. A. D'Hollander, Eugénie Romero, Cynthia Exilie, Kevin Cariou, Corinne Minard
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre), Immunologie des maladies virales, auto-immunes, hématologiques et bactériennes (IMVA-HB), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris-Saclay, Médicaments et Technologies pour la Santé (MTS), Université Paris-Saclay-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Ecologie et Evolution de la Résistance aux Antibiotiques / Ecology and Evolution of Antibiotics Resistance (EERA), Institut Pasteur [Paris] (IP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), This work was supported by the Laboratory of Excellence in Research on Medication and Innovative Therapeutics (LERMIT, grant ANR-10-LABX-33 under the program Investissements d’Avenir ANR-11-IDEX-0003-01), the FCS Campus Paris-Saclay pre-maturation program (project Inhibase), the SATT Paris-Saclay (project CARBAMAT), the JPIAMR transnational project DesInMBL (grant ANR-14-JAMR-0002) and the Région Ile-de-France (DIM Malinf). The authors also thank CNRS, AP-HP, Université Paris-Saclay, and ICSN, for financial support., ANR-10-LABX-0033,LERMIT,Research Laboratory on Drugs and Therapeutic Innovation(2010), ANR-11-IDEX-0003,IPS,Idex Paris-Saclay(2011), ANR-14-JAMR-0002,DesInMBL,Structure-guided design of pan inhibitors of metallo-ß-lactamases(2014), Institut Pasteur [Paris]-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Cariou, Kevin, Research Laboratory on Drugs and Therapeutic Innovation - - LERMIT2010 - ANR-10-LABX-0033 - LABX - VALID, Idex Paris-Saclay - - IPS2011 - ANR-11-IDEX-0003 - IDEX - VALID, programmation conjointe européenne sur la résistance antimicrobienne - Structure-guided design of pan inhibitors of metallo-ß-lactamases - - DesInMBL2014 - ANR-14-JAMR-0002 - JPI AMR - VALID
المصدر: European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, 2021, 219, ⟨10.1016/j.ejmech.2021.113418⟩
European Journal of Medicinal Chemistry, Elsevier, 2021, 219, ⟨10.1016/j.ejmech.2021.113418⟩مصطلحات موضوعية: Imipenem, Non covalent, Antibiotics, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, medicine.disease_cause, 01 natural sciences, Broad spectrum, Catalytic Domain, Drug Discovery, polycyclic compounds, OXA-48, chemistry.chemical_classification, 0303 health sciences, biology, Escherichia coli Proteins, General Medicine, Ynamides, Anti-Bacterial Agents, Molecular Docking Simulation, Microsomes, Liver, beta-Lactamase Inhibitors, medicine.drug, Gram-negative bacteria, Carbapenemase inhibitors, medicine.drug_class, Stereochemistry, Azetidinimines, [CHIM.THER] Chemical Sciences/Medicinal Chemistry, Microbial Sensitivity Tests, NDM-1, beta-Lactamases, Bacterial resistance, KPC-2, Cell Line, Inhibitory Concentration 50, Structure-Activity Relationship, 03 medical and health sciences, Antibiotic resistance, Gram-Negative Bacteria, medicine, Humans, Escherichia coli, Cell Proliferation, 030304 developmental biology, Pharmacology, Binding Sites, 010405 organic chemistry, Organic Chemistry, biochemical phenomena, metabolism, and nutrition, biology.organism_classification, 0104 chemical sciences, Enzyme, chemistry, Azetidines
وصف الملف: application/pdf
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المؤلفون: Linda Tlili, Thierry Naas, Eddy Elisée, Robert H. Dodd, Mohamed Benchekroun, Agustin Zavala, Eugénie Romero, Alain Pruvost, Corinne Minard, Agathe C.A. D'Hollander, Kevin Cariou, Saoussen Oueslati, Bogdan I. Iorga, Cynthia Exilie, Sandrine Ventre, Kamsana Vijayakumar, Edithe Selwa, Pascal Retailleau, Laetitia Nguyen
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Institut de Chimie du CNRS (INC)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS), Structure, Dynamique, Fonction Et Expression Des Beta-Lactamases À Large Spectre, Université Paris-Sud - Paris 11 - Faculté de médecine (UP11 UFR Médecine), Université Paris-Sud - Paris 11 (UP11)-Université Paris-Sud - Paris 11 (UP11)-Centre National de Référence de la Résistance aux Antibiotiques (CNR), Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon)-Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), CEA- Saclay (CEA), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
مصطلحات موضوعية: Imipenem, Gram-negative bacteria, medicine.drug_class, Stereochemistry, Non covalent, Antibiotics, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, medicine.disease_cause, 01 natural sciences, 03 medical and health sciences, Broad spectrum, Antibiotic resistance, polycyclic compounds, medicine, Escherichia coli, 030304 developmental biology, chemistry.chemical_classification, 0303 health sciences, biology, 010405 organic chemistry, biology.organism_classification, 0104 chemical sciences, 3. Good health, Enzyme, chemistry, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6429d706c57db24e49ca06471b6ee68d
https://hal.archives-ouvertes.fr/hal-02998861/document -
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المؤلفون: Sandrine Ventre, Eugénie Romero, Corinne Minard, Mohamed Benchekroun, Pascal Retailleau, Robert H. Dodd, Kevin Cariou
المساهمون: Institut de Chimie des Substances Naturelles (ICSN), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC), Institut Parisien de Chimie Moléculaire (IPCM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (53), pp.12991-12994. ⟨10.1002/chem.201702545⟩مصطلحات موضوعية: chemistry.chemical_classification, Base (chemistry), 010405 organic chemistry, Stereochemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Staudinger synthesis, General Chemistry, 010402 general chemistry, 01 natural sciences, Catalysis, Cycloaddition, 0104 chemical sciences, chemistry, QD0241
وصف الملف: application/pdf
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المؤلفون: Cédric Simon, Geoffrey Gontard, Muriel Amatore, Etienne Derat, Marc Petit, Alejandro Rivera-Hernández, Sandrine Ventre, Marie-Hélène Tremblay, Corinne Aubert, Brendan J. Fallon
المساهمون: Institut Parisien de Chimie Moléculaire (IPCM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), CNRS, MRES, UPMC, CONACYT [252113], ANR-12-BS07-0031,CoCaCoLight,Activation de liaisons par des complexes de Cobalt(I) et fonctionnalisation assistée par la lumière(2012)
المصدر: Organic Letters
Organic Letters, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩
Organic Letters, American Chemical Society, 2016, 18 (17), pp.4242-4245. ⟨10.1021/acs.orglett.6b01987⟩مصطلحات موضوعية: 010405 organic chemistry, Hydrosilylation, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, chemistry.chemical_element, 010402 general chemistry, 01 natural sciences, Biochemistry, Combinatorial chemistry, 0104 chemical sciences, Catalysis, Cobalt catalyst, chemistry.chemical_compound, chemistry, Organic chemistry, Stereoselectivity, Physical and Theoretical Chemistry, Cobalt
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المؤلفون: Filip Petronijevic, David W. C. MacMillan, Sandrine Ventre
المصدر: ChemInform. 46
مصطلحات موضوعية: Chemistry, Decarboxylation, Halogenation, Photoredox catalysis, Organic chemistry, General Medicine
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المؤلفون: Sandrine Ventre, Filip Petronijevic, David W. C. MacMillan
مصطلحات موضوعية: chemistry.chemical_classification, Quenching (fluorescence), Halogenation, Hydrocarbons, Fluorinated, Molecular Structure, Radical, Carboxylic Acids, Photoredox catalysis, General Chemistry, Photochemical Processes, Biochemistry, Decarboxylation, Article, Catalysis, Colloid and Surface Chemistry, chemistry, Reagent, Yield (chemistry), Organic chemistry, Oxidation-Reduction, Alkyl
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba095e59cc7554e449a4283d94e77efc
https://europepmc.org/articles/PMC4862610/ -
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المؤلفون: Kevin Cariou, Corinne Minard, Pascal Retailleau, Robert H. Dodd, Eugénie Romero, Sandrine Ventre, Mohamed Benchekroun
المصدر: Chemistry - A European Journal. 23:12956-12956
مصطلحات موضوعية: Chemistry, Stereochemistry, Organic Chemistry, Staudinger synthesis, Cover (algebra), General Chemistry, Catalysis
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المؤلفون: Muriel Amatore, Sandrine Ventre, Marc Petit, Corinne Aubert, Etienne Derat
المصدر: ChemInform. 45
مصطلحات موضوعية: Cobalt catalyst, Scope (project management), Chemistry, Yield (chemistry), Organic chemistry, Stereoselectivity, General Medicine
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المؤلفون: Corinne Aubert, Peter L. Pauson, Muriel Amatore, Marc Petit, Sandrine Ventre
مصطلحات موضوعية: chemistry.chemical_classification, chemistry.chemical_compound, chemistry, Cyclopentadienyl complex, Polymer chemistry, Alkyne, chemistry.chemical_element, Solubility, Inert gas, Cyclopentadienylcobalt dicarbonyl, Cobalt, Carbon, Catalysis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3073babe4c48a37c6439fbe0e891fcad
https://doi.org/10.1002/047084289x.rd078.pub2 -
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المؤلفون: Marc Petit, Feriel Rekhroukh, Max Malacria, Muriel Amatore, Sandrine Ventre, Corinne Aubert, Cédric Simon
المصدر: ChemInform. 44
مصطلحات موضوعية: chemistry, Bicyclic molecule, Enediyne, chemistry.chemical_element, Substrate (chemistry), Chelation, General Medicine, Light activation, Cobalt, Combinatorial chemistry, Cycloaddition, Catalysis
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