المؤلفون: Gloria Rubiales, Cinzia Tesauro, María Fuertes, Endika Martin-Encinas, Asier Selas, Concepción Alonso, Francisco Palacios, Birgitta K. Knudssen

المصدر: Alonso, C, Fuertes, M, Martín-Encinas, E, Selas, A, Rubiales, G, Tesauro, C, Knudssen, B K & Palacios, F 2018, ' Novel topoisomerase I inhibitors. Syntheses and biological evaluation of phosphorus substituted quinoline derivates with antiproliferative activity ', European Journal of Medicinal Chemistry, vol. 149, pp. 225-237 . https://doi.org/10.1016/j.ejmech.2018.02.058

مصطلحات موضوعية: Phosphines, Phosphorus/chemistry, Antineoplastic Agents, 010402 general chemistry, 01 natural sciences, Stereocenter, Cell Proliferation/drug effects, Structure-Activity Relationship, chemistry.chemical_compound, DESIGN, Cell Line, Tumor, Drug Discovery, Humans, Structure–activity relationship, Dehydrogenation, MEDICINAL CHEMISTRY, DNA TOPOISOMERASES, Quinolines/chemistry, Cell Proliferation, Antiproliferative effect, Pharmacology, A549 cell, biology, 010405 organic chemistry, Chemistry, Topoisomerase, Topoisomerase I Inhibitors/chemical synthesis, Organic Chemistry, Quinoline, Phosphorated quinolines, Phosphorus, General Medicine, CANCER, Combinatorial chemistry, 0104 chemical sciences, Topoisomerase I, Enzyme inhibition, MULTICOMPONENT REACTIONS, DISCOVERY, Quinolines, biology.protein, COMPLEXES, Hydrogenation, Topoisomerase I Inhibitors, Drug Screening Assays, Antitumor, Selectivity, Phosphine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f6015f40e306409f613037ba63637fa
https://doi.org/10.1016/j.ejmech.2018.02.058

المؤلفون: Bensikaddour, Hayet, Fa, Nathalie, Burton, Ingrid, Deleu, Magali, Lins, Laurence, Schanck, Andre, Brasseur, Robert, Dufrene, Yves F, Goormaghtigh, Erik, Mingeot-Leclercq, Marie*-Paule

المصدر: Biophysical Journal, 94 (8), 3035-46 (2008)

مصطلحات موضوعية: Anti-Bacterial Agents/chemistry, Aza Compounds/chemistry, Ciprofloxacin/chemistry, Complex Mixtures/chemistry, Fluoroquinolones/chemistry, Membrane Lipids/chemistry, Membrane Microdomains/chemistry, Microscopy, Atomic Force/methods, Molecular Conformation, Phase Transition, Phospholipids/chemistry, Quinolines/chemistry, Spectroscopy, Fourier Transform Infrared/methods, Surface Properties, Life sciences, Biochemistry, biophysics & molecular biology, Sciences du vivant, Biochimie, biophysique & biologie moléculaire

Relation: urn:issn:0006-3495; urn:issn:1542-0086

URL الوصول: https://orbi.uliege.be/handle/2268/63309

المؤلفون: Roberta Mazzone, Piero Picci, Katia Scotlandi, Michela Pasello, Patrizia Nanni, Giordano Nicoletti, Maria Cristina Manara, Antonello Mai, Clara Guerzoni, Camilla Cristalli, Pier Luigi Lollini, Lorena Landuzzi, Sergio Valente, Giulia Stazi, Paola B. Arimondo, Clemens Zwergel

المساهمون: Istituto Ortopedico Rizzoli [Bologna, Italy], Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Centre National de la Recherche Scientifique (CNRS), Department of Medicinal Chemistry and Technologies, Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], This work was funded by AIRC (IG 18451 to K. Scotlandi, IG 19162 to A. Mai), the Italian Ministry of Health (TRANSCAN_ project TORPEDO_ER-2015-23604059 to K. Scotlandi), Progetto Ateneo Sapienza (to A. Mai), PRIN 2016 (prot 20152TE5PK to A. Mai), and the NIH (R01GM114306 to A. Mai)., The authors thank Cristina Ghinelli for editing the manuscript., Manara, Maria Cristina, Valente, Sergio, Cristalli, Camilla, Nicoletti, Giordano, Landuzzi, Lorena, Zwergel, Clemen, Mazzone, Roberta, Stazi, Giulia, Arimondo, Paola B, Pasello, Michela, Guerzoni, Clara, Picci, Piero, Nanni, Patrizia, Lollini, Pier-Luigi, Mai, Antonello, Scotlandi, Katia

المصدر: Molecular Cancer Therapeutics
Molecular Cancer Therapeutics, American Association for Cancer Research, 2018, 17 (9), pp.1881-1892. ⟨10.1158/1535-7163.MCT-17-0818⟩

مصطلحات موضوعية: 0301 basic medicine, Male, patient-derived xenograft (PDX), MESH: Osteosarcoma/genetics, MESH: Antineoplastic Combined Chemotherapy Protocols/therapeutic use, Cellular differentiation, DNA Methyltransferase Inhibitor, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, chemotherapy, MESH: Mice, Knockout, 0302 clinical medicine, MESH: Osteosarcoma/drug therapy, Antineoplastic Combined Chemotherapy Protocols, MESH: Aminoquinolines/administration & dosage, MESH: Animals, MESH: Quinolines/chemistry, Enzyme Inhibitors, MESH: DNA (Cytosine-5-)-Methyltransferase 1/metabolism, Mice, Knockout, DNA methylation, Chemistry, 3. Good health, Tumor Burden, MESH: Benzamides/pharmacology, Gene Expression Regulation, Neoplastic, 030220 oncology & carcinogenesis, Benzamides, oncology, Aminoquinolines, Quinolines, MESH: Cisplatin/administration & dosage, MESH: Bone Neoplasms/metabolism, Osteosarcoma, MESH: Doxorubicin/administration & dosage, epigenetic, MESH: Bone Neoplasms/genetics, medicine.drug, DNA (Cytosine-5-)-Methyltransferase 1, musculoskeletal diseases, MESH: Aminoquinolines/pharmacology, MESH: Cell Line, Tumor, DNA damage, MESH: Gene Expression Regulation, Neoplastic/drug effects, MESH: Tumor Burden/genetics, MESH: Xenograft Model Antitumor Assays, Bone Neoplasms, [SDV.CAN]Life Sciences [q-bio]/Cancer, 03 medical and health sciences, Cell Line, Tumor, osteosarcoma, medicine, Animals, Humans, Doxorubicin, MESH: DNA (Cytosine-5-)-Methyltransferase 1/antagonists & inhibitors, MESH: Enzyme Inhibitors/chemistry, Cisplatin, MESH: Humans, Nucleoside inhibitor, medicine.disease, MESH: Enzyme Inhibitors/pharmacology, Xenograft Model Antitumor Assays, MESH: Male, MESH: Enzyme Inhibitors/administration & dosage, MESH: Bone Neoplasms/drug therapy, 030104 developmental biology, MESH: Osteosarcoma/metabolism, Cancer research, cancer research, MESH: DNA (Cytosine-5-)-Methyltransferase 1/genetics, MESH: Benzamides/administration & dosage, MESH: Tumor Burden/drug effects

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e55d5482d55dc2ed43ad6818ec4cbf60
https://hal.archives-ouvertes.fr/hal-02383680

المؤلفون: May C. Morris, Juan A. González-Vera, Ibon Alkorta, Francisco Fueyo-González, Marion Peyressatre, Rosario Herranz

المساهمون: Ministerio de Economía y Competitividad (España), Consejo Superior de Investigaciones Científicas (España), European Commission, Spanish National Research Council [Madrid] (CSIC), Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM), Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM), Instituto de Quimica Médica (CSIC), Consejo Superior de Investigaciones Científicas [Madrid] (CSIC)

المصدر: Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2016, 52 (62), pp.9652-9655. ⟨10.1039/c6cc04566a⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname

مصطلحات موضوعية: Scaffold, Stereochemistry, MESH: Molecular Structure, Peptide, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, 010402 general chemistry, 01 natural sciences, Catalysis, Materials Chemistry, medicine, Humans, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, MESH: Fluorescent Dyes / chemistry, MESH: Quinolines / chemistry, Fluorescent Dyes, chemistry.chemical_classification, MESH: Humans, Molecular Structure, 010405 organic chemistry, Cyclin-dependent kinase 5, Solvatochromism, Metals and Alloys, Cyclin-Dependent Kinase 5, General Chemistry, [SDV.SP]Life Sciences [q-bio]/Pharmaceutical sciences, medicine.disease, female genital diseases and pregnancy complications, eye diseases, 3. Good health, 0104 chemical sciences, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, chemistry, Ceramics and Composites, Biophysics, MESH: Cyclin-Dependent Kinase 5 / chemistry, Quinolines, Solvents, Glioblastoma

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a6da4b43671d415341ed577718974dd
https://pubmed.ncbi.nlm.nih.gov/27383006

المؤلفون: Françoise Van Bambeke, Paul M. Tulkens, Sandrine Lemaire

المساهمون: UCL - SSS/LDRI - Louvain Drug Research Institute

المصدر: Antimicrobial Agents and Chemotherapy, Vol. 55, no. 2, p. 649-658 (2011)

مصطلحات موضوعية: Staphylococcus aureus, Moxifloxacin, Staphylococcal Infections - microbiology, Microbial Sensitivity Tests, medicine.disease_cause, Staphylococcal infections, Models, Biological, Monocytes, Cell Line, Microbiology, Mice, chemistry.chemical_compound, Anti-Infective Agents, Staphylococcus aureus - drug effects, metabolism, Aza Compounds - chemistry, pharmacokinetics, pharmacology, medicine, Extracellular, Animals, Humans, Pharmacology (medical), Pharmacology, Aza Compounds, Monocytes - metabolism, microbiology, biology, Macrophages, Anti-Infective Agents - chemistry, pharmacokinetics, pharmacology, Quinolines - chemistry, pharmacokinetics, pharmacology, Hydrogen-Ion Concentration, Staphylococcal Infections, biology.organism_classification, medicine.disease, Culture Media, Infectious Diseases, chemistry, Susceptibility, Cell culture, Fluoroquinolones - chemistry, pharmacokinetics, pharmacology, Macrophages - metabolism, Quinolines, Delafloxacin, Culture Media - chemistry, Bacteria, Intracellular, Fluoroquinolones, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f8112214dcc534fc3e5621bbe7cab9e
https://doi.org/10.1128/aac.01201-10

المؤلفون: Sarah K. Volkman, Lise Musset, Eric Legrand, Stanislaw J. Gabryszewski, Dyann F. Wirth, Béatrice Volney, Eli L. Moss, Stéphane Pelleau, Satish K. Dhingra, Daniel E. Neafsey, David A. Fidock, Jessica Casteras

المساهمون: Laboratoire de Parasitologie, Centre National de Référence du Paludisme - Région Antilles-Guyane, Institut Pasteur de la Guyane - Réseau International des Instituts Pasteur - WHO Collaborating Center for Surveillance of Antimalarial Drug Resistance, Broad Institute of MIT and Harvard (BROAD INSTITUTE), Broad Institute of MIT and Harvard, Department of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, Harvard School of Public Health, This work was supported by European Commission Grant REGPOT-CT-2011-285837-430 STRonGer (to S.P.), AgenceNationale de la Recherche Investissements d’Avenir Grant ANR-10-LABX-25-01(to S.P. and L.M.), NIH Grants R01AI50234 (to D.A.F.) and R01AI109023 (to D.A.F.),and the Institut de Veille Sanitaire. Sequencing was supported, in part, byNational Institute of Allergy and Infectious Diseases, NIH, Department ofHealth and Human Services Contract HHSN272200900018C., ANR-10-LABX-25-01/10-LABX-0025, CEBA, CEnter of the study of Biodiversity in Amazonia(2010), European Project : 285837, EC:FP7:REGPOT, FP7-REGPOT-2011-1, STRONGER(2011), Centre National de Référence du Paludisme [Cayenne, Guyane française] (CNR - laboratoire associé), Institut Pasteur de la Guyane, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Columbia University College of Physicians and Surgeons, ANR-10-LABX-0025,CEBA,CEnter of the study of Biodiversity in Amazonia(2010), European Project: 285837,EC:FP7:REGPOT,FP7-REGPOT-2011-1,STRONGER(2011), Centre National de Référence du Paludisme [Cayenne, Guyane française] (CNR), Centre National de Référence du Paludisme - Laboratoire de parasitologie [Cayenne, Guyane française] (CNR)

المصدر: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2015, 112 (37), pp.11672-7
Proceedings of the National Academy of Sciences of the United States of America, 2015, 112 (37), pp.11672-11677. ⟨10.1073/pnas.1507142112⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2015, 112 (37), pp.11672-11677. ⟨10.1073/pnas.1507142112⟩

مصطلحات موضوعية: [SDV]Life Sciences [q-bio], Protozoan Proteins, Drug resistance, MESH: Genetic Markers, MESH: Genotype, Chloroquine, Genotype, [SDV.SPEE] Life Sciences [q-bio]/Public Health and Epidemiology, MESH: Quinolines/chemistry, MESH: Inhibitory Concentration 50, Genetics, education.field_of_study, Multidisciplinary, biology, MESH: Chloroquine/therapeutic use, Biological Sciences, MESH: Malaria/drug therapy, 3. Good health, [SDV] Life Sciences [q-bio], [SDV.MP.PAR] Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology, medicine.drug, PfCRT, MESH: Plasmodium falciparum/drug effects, Population, Plasmodium falciparum, MESH: Plasmodium falciparum/genetics, malaria, MESH: Membrane Transport Proteins/genetics, MESH: Phenotype, Evolution, Molecular, Piperaquine, evolution, MESH: Evolution, Molecular, MESH: French Guiana, parasitic diseases, medicine, Humans, MESH: Genome, [SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/Parasitology, Allele, education, MESH: Prevalence, MESH: Principal Component Analysis, drug resistance, MESH: Humans, MESH: Alleles, Membrane Transport Proteins, MESH: Retrospective Studies, MESH: Haplotypes, biology.organism_classification, medicine.disease, MESH: Protozoan Proteins/genetics, Mutation, MESH: Mutation, MESH: Drug Resistance/genetics, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Malaria

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98f1f82c8002d2b8ac21235f6b72c4a9
https://hal-pasteur.archives-ouvertes.fr/pasteur-01229321/document

المؤلفون: Francisco Palma-Cerda, Francine Acher, Christine Tran, Morgane Petit, Hamid Dhimane, Peter I. Dalko, Mireille Blanchard-Desce, Thibault Gallavardin, Thomas Roger, David Ogden

المساهمون: Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques (LCBPT - UMR 8601), Université Paris Descartes - Paris 5 (UPD5)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Laboratoire de physiologie cérébrale (LPC - UMR 8118), Université Paris Diderot - Paris 7 (UPD7)-Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Chimie et Photonique Moléculaires (CPM), Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS), Gallavardin, Thibault, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS)

المصدر: Organic Letters
Organic Letters, 2012, 14 (24), pp.6366-6369. ⟨10.1021/ol3031704⟩
Organic Letters, American Chemical Society, 2012, 14 (24), pp.6366-6369. ⟨10.1021/ol3031704⟩

مصطلحات موضوعية: Stereochemistry, Quinolines/chemistry, Glutamates/chemistry, 010402 general chemistry, Photochemistry, 01 natural sciences, Biochemistry, chemistry.chemical_compound, Structure-Activity Relationship, Two-photon excitation microscopy, Glutamates, [CHIM] Chemical Sciences, Structure–activity relationship, Molecule, [CHIM]Chemical Sciences, Substitution effect, Physical and Theoretical Chemistry, Photons, Photolysis, Molecular Structure, 010405 organic chemistry, [CHIM.ORGA]Chemical Sciences/Organic chemistry, Organic Chemistry, Quinoline, Photodissociation, Glutamate receptor, [CHIM.ORGA] Chemical Sciences/Organic chemistry, 3. Good health, 0104 chemical sciences, chemistry, Quinolines, Derivative (chemistry)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e8138397f55f8fe897e91594a2237e
https://hal-normandie-univ.archives-ouvertes.fr/hal-02383436

المؤلفون: Benjamin D. Bax, Pan F. Chan, Michael M. Hann, Michael N. Gwynn, Daniel R. Gentry, Ceri J. Lewis, Jo J. Jones, Claus Spitzfaden, Andrew P. Fosberry, Martin Hibbs, Earl May, Kristin K. Brown, Alexandre Wohlkonig, Drake S. Eggleston, Onkar M. P. Singh, Alan Joseph Hennessy, Andrew J. Theobald, Fabrice Gorrec, Martin R. Saunders, Anthony Shillings, Emma J. Jones, Carol Shen, Neil D. Pearson, Jianzhong Huang, Ilaria Giordano

المساهمون: Department of Bio-engineering Sciences, Structural Biology Brussels

مصطلحات موضوعية: Models, Molecular, Gepotidacin, Staphylococcus aureus, Stereochemistry, Protein Conformation, Drug Resistance, Anti-Bacterial Agents/chemistry, Quinolones, Manganese/metabolism, Arginine, Crystallography, X-Ray, DNA gyrase, Apoenzymes, Arginine/metabolism, Ciprofloxacin, Catalytic Domain, Escherichia coli, Topoisomerase II Inhibitors, Ciprofloxacin/chemistry, DNA Gyrase/chemistry, DNA, Superhelical/chemistry, Escherichia coli/enzymology, DNA Cleavage, DNA/chemistry, Quinolines/chemistry, Antibacterial agent, Aspartic Acid, Manganese, Multidisciplinary, Binding Sites, biology, Apoenzymes/chemistry, Drug discovery, DNA, Superhelical, Topoisomerase, DNA, Staphylococcus aureus/enzymology, Structure-activity relationship, Quinolones/chemistry, Anti-Bacterial Agents, Biochemistry, DNA Gyrase, Drug Design, biology.protein, Quinolines, Primase, Topoisomerase-II Inhibitor, Type II topoisomerase, Aspartic Acid/metabolism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ea159ed95a9dbead771494c8d86bdb2
https://doi.org/10.1038/nature09197

المؤلفون: Natascha Chavain, Christophe Biot, Cheikh M. N'Diaye, Patricia Melnyk, Jamal Khalife, Alain Pellet, Christian Jarry, Jacques Brocard, Lydie Pelinski, Isabelle Forfar-Bares, Daniel Dive, Wassim Daher, Bruno Pradines, Laurent Fraisse

المساهمون: Unité de Catalyse et Chimie du Solide - UMR 8181 (UCCS), Centrale Lille Institut (CLIL)-Université d'Artois (UA)-Centrale Lille-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Lille, Schistosomiase, paludisme et inflammation, Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé, Université Lille 2 - Faculté de Médecine, Université de Lille, Institut de Médecine Tropicale du Service de Santé des Armées (IMTSSA), Service de Santé des Armées, SANOFI Recherche, Pharmacochimie (EA2962), Université Bordeaux Segalen - Bordeaux 2, This work was supported by Sanofi Aventis (fellowship attributed to W.D.), by the 'Fondation des Treilles' (fellowship attributed to W.D.) by the CNRS, by the Universités de Lille I and Lille II, and by the Inserm. A BDI fellowship from CNRS and Region Nord-Pas-de-Calais to N.C. is also gratefully acknowledged., C.B. thanks Timothy J. Egan for stimulating discussions and careful reading of the manuscript. L. Maciejewski is acknowledged for helpful discussions. I. Ricard, L. Cattiaux, H. Kalamou, and D. Lamberton are acknowledged for their expert technical intervention., Université d'Artois (UA)-Centrale Lille-Institut de Chimie du CNRS (INC)-Université de Lille-Centre National de la Recherche Scientifique (CNRS), Faculté de Médecine Henri Warembourg - Université de Lille

المصدر: Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2006, 49, pp.4707-4714. ⟨10.1021/jm060259d⟩
Journal of Medicinal Chemistry, 2006, 49, pp.4707-4714. ⟨10.1021/jm060259d⟩

مصطلحات موضوعية: MESH: Ferrous Compounds/chemistry, Metallocenes, MESH: Ferrous Compounds/chemical synthesis, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, MESH: Parasitic Sensitivity Tests, MESH: Quinolines/pharmacology, 01 natural sciences, Chemical synthesis, chemistry.chemical_compound, MESH: Structure-Activity Relationship, Parasitic Sensitivity Tests, MESH: Antimalarials/pharmacology, Drug Discovery, MESH: Aminoquinolines, Moiety, MESH: Animals, MESH: Quinolines/chemistry, MESH: Quinolines/chemical synthesis, biology, Chloroquine, MESH: Chloroquine/chemistry, 3. Good health, [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology, Covalent bond, Lipophilicity, Aminoquinolines, Quinolines, Molecular Medicine, MESH: Antimalarials/chemical synthesis, Metallocene, Hemeproteins, MESH: Plasmodium falciparum/drug effects, Stereochemistry, MESH: Hemeproteins/antagonists & inhibitors, Plasmodium falciparum, 010402 general chemistry, Antimalarials, Structure-Activity Relationship, MESH: Antimalarials/chemistry, Animals, Structure–activity relationship, Ferrous Compounds, MESH: Hemeproteins/chemical synthesis, 010405 organic chemistry, biology.organism_classification, MESH: Ferrous Compounds/pharmacology, 0104 chemical sciences, Ferrocene, chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d48cbd66cfa5d3e1dec078dd4c02cae9
https://hal.archives-ouvertes.fr/hal-00097346

المؤلفون: Dejaegher, Bieke, Dhooghe, L., Goodarzi, M, Apers, Sandra, Pieters, Luc, Vander Heyden, Yvan

المصدر: Analytica chimica acta, 705 (1-2

مصطلحات الفهرس: Sciences bio-médicales et agricoles, Alkaloids -- chemistry -- pharmacology, Antimalarials -- chemistry -- pharmacology, Discriminant Analysis, Hemeproteins -- antagonists & inhibitors -- metabolism, Humans, Least-Squares Analysis, Malaria -- drug therapy, Models, Biological, Plasmodium falciparum -- drug effects, Quantitative Structure-Activity Relationship, Quinolines -- chemistry -- pharmacology, Support Vector Machines, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article

URL: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/191703
http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL