نتائج البحث - "Loiseau, Philippe M."

1

دورية أكاديمية

Effect of Phlebotomus papatasi on the fitness, infectivity and antimony-resistance phenotype of antimony-resistant Leishmania major Mon-25

المؤلفون: Mekarnia, Nalia, Benallal, Kamal-Eddine, Sádlová, Jovana, Vojtková, Barbora, Mauras, Aurélie, Imbert, Nicolas, Longhitano, Maryline, Harrat, Zoubir, Volf, Petr, Loiseau, Philippe, M, Cojean, Sandrine

المساهمون: Epidémiosurveillance de protozooses à transmission alimentaire et vectorielle (ESCAPE), Université de Reims Champagne-Ardenne (URCA)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail (ANSES)

المصدر: ISSN: 2211-3207 ; International journal for parasitology. Drugs and drug resistance ; https://hal.univ-reims.fr/hal-04632483Test ; International journal for parasitology. Drugs and drug resistance, 2024, 25, pp.100554. ⟨10.1016/j.ijpddr.2024.100554⟩.

مصطلحات موضوعية: Leishmania major Phlebotomus papatasi, experimental infection Fitness Virulence Antimony resistance, [SDV.EE.SANT]Life Sciences [q-bio]/Ecology, environment/Health, [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases, [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology

العلاقة: hal-04632483; https://hal.univ-reims.fr/hal-04632483Test; https://hal.univ-reims.fr/hal-04632483/documentTest; https://hal.univ-reims.fr/hal-04632483/file/1-s2.0-S2211320724000356-main.pdfTest

الإتاحة: https://doi.org/10.1016/j.ijpddr.2024.100554Test
https://hal.univ-reims.fr/hal-04632483Test
https://hal.univ-reims.fr/hal-04632483/documentTest
https://hal.univ-reims.fr/hal-04632483/file/1-s2.0-S2211320724000356-main.pdfTest

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2

دورية أكاديمية

Chemoselective Synthesis and Anti-Kinetoplastidal Properties of 2,6-Diaryl-4H-tetrahydro-thiopyran-4-one S-Oxides: Their Interplay in a Cascade of Redox Reactions from Diarylideneacetones

المؤلفون: Gendron, Thibault, Lanfranchi, Don Antoine, Wenzel, Nicole, I, Kessedjian, Hripsimée, Jannack, Beate, Maes, Louis, Cojean, Sandrine, Müller, Thomas, J J, Loiseau, Philippe, M, Davioud-Charvet, Elisabeth

المساهمون: Department of Chemistry UCL, London, University College of London London (UCL), Laboratoire d'innovation moléculaire et applications (LIMA), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Universität Heidelberg Heidelberg = Heidelberg University, University of Antwerp (UA), Biomolécules : Conception, Isolement, Synthèse (BioCIS), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), AP-HP - Hôpital Bichat - Claude Bernard Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Friedrich-Loeffler-Institut (FLI)

المصدر: ISSN: 1420-3049 ; Molecules ; https://hal.science/hal-04583951Test ; Molecules, 2024, 29 (7), pp.1620. ⟨10.3390/molecules29071620⟩.

مصطلحات موضوعية: anti-kinetoplastid, drug metabolites, Michael acceptor, redox, sulfide, sulfone, sulfoxide, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, [SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology

العلاقة: hal-04583951; https://hal.science/hal-04583951Test; https://hal.science/hal-04583951/documentTest; https://hal.science/hal-04583951/file/molecules-29-01620-v2-2.pdfTest

الإتاحة: https://doi.org/10.3390/molecules29071620Test
https://hal.science/hal-04583951Test
https://hal.science/hal-04583951/documentTest
https://hal.science/hal-04583951/file/molecules-29-01620-v2-2.pdfTest

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3

دورية أكاديمية

The Synthesis of 2′-Hydroxychalcones under Ball Mill Conditions and Their Biological Activities

المؤلفون: Abid, Imen, Moslah, Wassim, Cojean, Sandrine, Imbert, Nicolas, Loiseau, Philippe, M, Chamayou, Alain, Srairi-Abid, Najet, Calvet, Rachel, Baltas, Michel

المساهمون: Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Centre de recherche d'Albi en génie des procédés des solides divisés, de l'énergie et de l'environnement (RAPSODEE), Centre National de la Recherche Scientifique (CNRS)-IMT École nationale supérieure des Mines d'Albi-Carmaux (IMT Mines Albi), Institut Mines-Télécom Paris (IMT)-Institut Mines-Télécom Paris (IMT), Biomolécules, Venins et Applications Théranostiques Tunis, Institut Pasteur de Tunis, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Université de Tunis El Manar (UTM), Biomolécules : Conception, Isolement, Synthèse (BioCIS), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), AP-HP - Hôpital Bichat - Claude Bernard Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), New Antimalarial Molecules and Pharmacological Approaches (ERL1289), Centre d'investigation clinique de Toulouse (CIC 1436), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Pôle Santé publique et médecine publique CHU Toulouse, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Université Toulouse III - Paul Sabatier (UT3), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), CNRS, University Paul Sabatier, IMT Mines Albi, COST Action CA21111 “One Health drugs”, The authors would like to gratefully acknowledge the Region Occitanie (France) for thethesis grant (I.A.) (contract number 00090086/21012467), and the CNRS, University Paul Sabatier, and IMT Mines Albi for financial support. This collaborative study was initiated through the COST Action CA21111 “One Health drugs” that is acknowledged for its scientific activities.

المصدر: ISSN: 1420-3049 ; Molecules ; https://hal.science/hal-04550832Test ; Molecules, 2024, 29 (8), pp.1819. ⟨10.3390/molecules29081819⟩.

مصطلحات موضوعية: Ball mill mechanochemistry, Sustainable synthesis, Chalcones, Phenolics, Antiparasitic, Antitumoral, [CHIM.THER]Chemical Sciences/Medicinal Chemistry

العلاقة: hal-04550832; https://hal.science/hal-04550832Test; https://hal.science/hal-04550832/documentTest; https://hal.science/hal-04550832/file/Abid,%20The%20Synthesis%20of%2020-Hydroxychalcones,%202024.pdfTest

الإتاحة: https://doi.org/10.3390/molecules29081819Test
https://hal.science/hal-04550832Test
https://hal.science/hal-04550832/documentTest
https://hal.science/hal-04550832/file/Abid,%20The%20Synthesis%20of%2020-Hydroxychalcones,%202024.pdfTest

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4

دورية أكاديمية

1,2,3-triazenes and 1,2,3-triazoles as antileishmanial, antitrypanosomal, and antiplasmodial agents

المؤلفون: Seck, Insa, Ciss, Ismaïla, Diédhiou, Adama, Baldé, Mamadou, Ka, Seydou, Ba, Lalla, Ndoye, Samba, Figadère, Bruno, Seon-Meniel, Blandine, Gomez, Generosa, Cojean, Sandrine, Pomel, Sébastien, Loiseau, Philippe, M, Fall, Yagamare, Seck, Matar

المساهمون: Université Cheikh Anta Diop de Dakar Sénégal (UCAD), Université Amadou Mahtar Mbow (UAM), Biomolécules : Conception, Isolement, Synthèse (BioCIS), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), Universidade de Vigo

المصدر: ISSN: 1054-2523.

مصطلحات موضوعية: trypanosomiasis, leishmaniasis, malaria, antiparasitic activity, 1-2-3-triazene, 1-2-3-triazole, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, [SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology

العلاقة: hal-04284870; https://hal.science/hal-04284870Test; https://hal.science/hal-04284870/documentTest; https://hal.science/hal-04284870/file/NEW%201,2,3-triazenes%20and%201,2,3-triazoles%20AS%20Antileishmanial,%20ANTITRYPANOSOMal%20and%20antiplasmodial%20AGENTS%20%20MS%202.pdfTest

الإتاحة: https://doi.org/10.1007/s00044-022-02994-9Test
https://hal.science/hal-04284870Test
https://hal.science/hal-04284870/documentTest
https://hal.science/hal-04284870/file/NEW%201,2,3-triazenes%20and%201,2,3-triazoles%20AS%20Antileishmanial,%20ANTITRYPANOSOMal%20and%20antiplasmodial%20AGENTS%20%20MS%202.pdfTest

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5

دورية أكاديمية

Alkyl-Resorcinol Derivatives as Inhibitors of GDP-Mannose Pyrophosphorylase with Antileishmanial Activities

المؤلفون: Levaique, Hélène, Pamlard, Olivier, Apel, Cécile, Bignon, Jérôme, Arriola, Margaux, Kuhner, Robin, Awang, Khalijah, Loiseau, Philippe M., Litaudon, Marc, Pomel, Sébastien

المساهمون: CNRS, Centrale Lille, ENSCL, Univ. Artois, Université de Lille, Unité de Catalyse et Chimie du Solide (UCCS) - UMR 8181, Institut de Chimie des Substances Naturelles ICSN, Biomolécules : Conception, Isolement, Synthèse BioCIS, University of Malaya = Universiti Malaya Kuala Lumpur, Malaisie UM

وصف الملف: application/rdf+xml; charset=utf-8; application/pdf

العلاقة: Molecules; http://hdl.handle.net/20.500.12210/62061Test

الإتاحة: https://doi.org/20.500.12210/62061Test
https://hdl.handle.net/20.500.12210/62061Test

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6

دورية أكاديمية

Deciphering the mechanism of action of VP343, an antileishmanial drug candidate, in Leishmania infantum

المؤلفون: Obeid, Sameh, Berbel-Manaia, Eloisa, Nicolas, Valérie, Dennemont, Indira, Barbier, Julien, Cintrat, Jean-Christophe, Gillet, Daniel, Loiseau, Philippe M., Pomel, Sébastien

المصدر: iScience ; volume 26, issue 11, page 108144 ; ISSN 2589-0042

مصطلحات موضوعية: Multidisciplinary

الإتاحة: https://doi.org/10.1016/j.isci.2023.108144Test
https://api.elsevier.com/content/article/PII:S2589004223022216?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S2589004223022216?httpAccept=text/plainTest

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7

دورية أكاديمية

Nanoassemblies from amphiphilic Sb complexes target infection sites in models of visceral and cutaneous leishmaniases

المؤلفون: Lanza, Juliane Sousa, Carregal, Virginia, Ramos, Guilherme S., De Oliveira, Ana Carolina B., Demicheli, Cynthia, Rivas, Luis, Pomel, Sébastien, Loiseau, Philippe M., Frézard, Frédéric

المساهمون: Conselho Nacional de Desenvolvimento Científico e Tecnológico (Brasil), Fundação de Amparo a Pesquisa do Estado de Minas Gerais, Brazilian Synchrotron Light Laboratory/MCT, Agence Nationale de la Recherche (France), Ministerio de Ciencia e Innovación (España), Carregal, Virginia, De Oliveira, Ana Carolina B., Demicheli, Cynthia, Rivas, Luis, Pomel, Sébastien, Loiseau, Philippe M., Frézard, Frédéric

مصطلحات موضوعية: Amphiphilic complexeA, Antimony, Drug targeting, Leishmania, Leishmaniasis, Miltefosine, Nanoassemblies

العلاقة: Publisher's version; https://doi.org/10.3390/pharmaceutics14081743Test; Sí; Pharmaceutics 14 (8) 1743 (2022); http://hdl.handle.net/10261/296879Test

الإتاحة: https://doi.org/10.3390/pharmaceutics14081743Test
http://hdl.handle.net/10261/296879Test

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النص الكامل

8

دورية أكاديمية

Chemoselective Synthesis and Anti-Kinetoplastidal Properties of 2,6-Diaryl-4 H -tetrahydro-thiopyran-4-one S -Oxides: Their Interplay in a Cascade of Redox Reactions from Diarylideneacetones.

المؤلفون: Gendron, Thibault, Lanfranchi, Don Antoine, Wenzel, Nicole I., Kessedjian, Hripsimée, Jannack, Beate, Maes, Louis, Cojean, Sandrine, Müller, Thomas J. J., Loiseau, Philippe M., Davioud-Charvet, Elisabeth

المصدر: Molecules; Apr2024, Vol. 29 Issue 7, p1620, 25p

مصطلحات موضوعية: OXIDATION-reduction reaction, SULFONE derivatives, TRYPANOSOMA brucei, REACTIVE oxygen species, POLYMERS, DOUBLE bonds, PHOSPHINE oxides, SULFOXIDES

النص الكامل

9

دورية أكاديمية

Design of Anti-infectious Agents from Lawsone in a Three-Component Reaction with Aldehydes and Isocyanides

المؤلفون: Koumpoura, Christina, L, Nguyen, Michel, Bijani, Christian, Vendier, Laure, Salina, Elena, G, Buroni, Silvia, Degiacomi, Giulia, Cojean, Sandrine, Loiseau, Philippe, M, Benoit-Vical, Françoise, García-Sosa, Alfonso, T, Robert, Anne, Baltas, Michel

المساهمون: Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), New Antimalarial Molecules and Pharmacological Approaches (ERL1289), Centre d'investigation clinique de Toulouse (CIC 1436), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Pôle Santé publique et médecine publique CHU Toulouse, Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Université Toulouse III - Paul Sabatier (UT3), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)-Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Russian Academy of Sciences Moscow (RAS), Dipartimento di Biologia e Biotecnologie "Lazzaro Spallanzani" = Department of Biology and Biotechnology Univ di Pavia (DBB UNIPV), Università degli Studi di Pavia = University of Pavia (UNIPV), Biomolécules : Conception, Isolement, Synthèse (BioCIS), Institut de Chimie - CNRS Chimie (INC-CNRS)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)-CY Cergy Paris Université (CY), University of Tartu, Centre National de la Recherche Scientifique (CNRS), Université Paul Sabatier, Institut National de la Santé et de la Recherche Médicale (INSERM), Fondation pour la Recherche Médicale (FRM), Paris Saclay University, Estonian Research Council, Italian Ministry of Education, University and Research (MIUR), University of Pavia

المصدر: ISSN: 2470-1343 ; ACS Omega ; https://hal.science/hal-03818601Test ; ACS Omega, 2022, 7 (40), pp.35635-35655. ⟨10.1021/acsomega.2c03421⟩.

مصطلحات موضوعية: Aldehydes, Carbon, Inorganic carbon compounds, Multicomponent reactions, Reaction products, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology

العلاقة: hal-03818601; https://hal.science/hal-03818601Test; https://hal.science/hal-03818601/documentTest; https://hal.science/hal-03818601/file/Koumpoura,%20Design%20of%20Anti-infectious%20Agents,%202022.pdfTest

الإتاحة: https://doi.org/10.1021/acsomega.2c03421Test
https://hal.science/hal-03818601Test
https://hal.science/hal-03818601/documentTest
https://hal.science/hal-03818601/file/Koumpoura,%20Design%20of%20Anti-infectious%20Agents,%202022.pdfTest

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