Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Beteck RM"" wg kryterium: Autor

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-10 z 10
    Tytuł:
    Arylnitro monocarbonyl curcumin analogues: Synthesis and in vitro antitubercular evaluation.
    Autorzy:
    du Preez C; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Legoabe LJ; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Jordaan A; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory, South Africa.
    Jesumoroti OJ; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Warner DF; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory, South Africa.; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Rondebosch, South Africa.; Faculty of Health Sciences, Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), University of Cape Town, Rondebosch, South Africa.
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Pokaż więcej
    Źródło:
    Chemical biology & drug design [Chem Biol Drug Des] 2023 Mar; Vol. 101 (3), pp. 717-726. Date of Electronic Publication: 2022 Nov 17.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Curcumin*
    Mycobacterium tuberculosis*
    Antitubercular Agents/pharmacology ; Structure-Activity Relationship ; Microbial Sensitivity Tests
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Assessment of the Activity of Decoquinate and Its Quinoline- O -Carbamate Derivatives against Toxoplasma gondii In Vitro and in Pregnant Mice Infected with T. gondii Oocysts.
    Autorzy:
    Ramseier J; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.
    Imhof D; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.; Graduate School for Cellular and Biomedical Sciences, University of Bern, Mittelstrasse 43, 3012 Bern, Switzerland.
    Anghel N; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.; Graduate School for Cellular and Biomedical Sciences, University of Bern, Mittelstrasse 43, 3012 Bern, Switzerland.
    Hänggeli K; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.; Graduate School for Cellular and Biomedical Sciences, University of Bern, Mittelstrasse 43, 3012 Bern, Switzerland.
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, Faculty of Health Sciences, North-West University, Potchefstroom 2520, South Africa.
    Balmer V; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.
    Ortega-Mora LM; SALUVET, Animal Health Department, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.
    Sanchez-Sanchez R; SALUVET, Animal Health Department, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.
    Ferre I; SALUVET, Animal Health Department, Faculty of Veterinary Sciences, Complutense University of Madrid, Ciudad Universitaria s/n, 28040 Madrid, Spain.
    Haynes RK; Centre of Excellence for Pharmaceutical Sciences, Faculty of Health Sciences, North-West University, Potchefstroom 2520, South Africa.
    Hemphill A; Institute of Parasitology, Vetsuisse Faculty, Department of Infectious Diseases and Pathobiology, University of Bern, Länggass-Strasse 122, 3012 Bern, Switzerland.
    Pokaż więcej
    Źródło:
    Molecules (Basel, Switzerland) [Molecules] 2021 Oct 22; Vol. 26 (21). Date of Electronic Publication: 2021 Oct 22.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Carbamates*/chemistry
    Antiprotozoal Agents/*pharmacology
    Decoquinate/*pharmacology
    Quinolines/*pharmacology
    Toxoplasma/*drug effects
    Toxoplasmosis, Animal/*drug therapy
    Toxoplasmosis, Animal/*parasitology
    Animals ; Antiprotozoal Agents/chemistry ; Decoquinate/analogs & derivatives ; Decoquinate/chemistry ; Disease Models, Animal ; Female ; Infectious Disease Transmission, Vertical/prevention & control ; Mice ; Molecular Structure ; Oocysts/drug effects ; Pregnancy ; Quinolines/chemistry ; Toxoplasma/ultrastructure
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Chemical Classes Presenting Novel Antituberculosis Agents Currently in Different Phases of Drug Development: A 2010-2020 Review.
    Autorzy:
    Angula KT; Centre of Excellence for Pharmaceutical Sciences (Pharmacen), North-West University, Potchefstroom 2520, South Africa.
    Legoabe LJ; Centre of Excellence for Pharmaceutical Sciences (Pharmacen), North-West University, Potchefstroom 2520, South Africa.
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences (Pharmacen), North-West University, Potchefstroom 2520, South Africa.
    Pokaż więcej
    Źródło:
    Pharmaceuticals (Basel, Switzerland) [Pharmaceuticals (Basel)] 2021 May 13; Vol. 14 (5). Date of Electronic Publication: 2021 May 13.
    Typ publikacji:
    Journal Article; Review
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
    Tytuł:
    Easy-To-Access Quinolone Derivatives Exhibiting Antibacterial and Anti-Parasitic Activities.
    Autorzy:
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom 2520, South Africa.
    Jordaan A; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, Faculty of Health Sciences, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town 7925, South Africa.
    Seldon R; SAMRC Drug Discovery and Development Research Unit, University of Cape Town, Cape Town 7700, South Africa.
    Laming D; Centre for Chemico- and Biomedicinal Research, Rhodes University, Makhanda 6140, South Africa.
    Hoppe HC; Centre for Chemico- and Biomedicinal Research, Rhodes University, Makhanda 6140, South Africa.; Department of Biochemistry and Microbiology, Faculty of Science, Rhodes University, Makhanda 6140, South Africa.
    Warner DF; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, Faculty of Health Sciences, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town 7925, South Africa.; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Cape Town 7925, South Africa.
    Khanye SD; Centre for Chemico- and Biomedicinal Research, Rhodes University, Makhanda 6140, South Africa.; Division of Pharmaceutical Chemistry, Faculty of Pharmacy, Rhodes University, Makhanda 6140, South Africa.
    Pokaż więcej
    Źródło:
    Molecules (Basel, Switzerland) [Molecules] 2021 Feb 20; Vol. 26 (4). Date of Electronic Publication: 2021 Feb 20.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Anti-Bacterial Agents/*pharmacology
    Antiprotozoal Agents/*pharmacology
    Quinolones/*pharmacology
    Acinetobacter baumannii/drug effects ; Anti-Bacterial Agents/chemical synthesis ; Anti-Bacterial Agents/chemistry ; Antiprotozoal Agents/chemical synthesis ; Antiprotozoal Agents/chemistry ; Dose-Response Relationship, Drug ; Microbial Sensitivity Tests ; Molecular Structure ; Parasitic Sensitivity Tests ; Plasmodium falciparum/drug effects ; Quinolones/chemical synthesis ; Quinolones/chemistry ; Staphylococcus aureus/drug effects ; Trypanosoma brucei brucei/drug effects
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    6-Nitro-1-benzylquinolones exhibiting specific antitubercular activity.
    Autorzy:
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Jordaan A; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory, South Africa.
    Swart T; Department of Biochemistry and Microbiology, Rhodes University, Grahamstown, South Africa.
    Van Der Kooy F; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Warner DF; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory, South Africa.; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Rondebosch, South Africa.; Wellcome Centre for Infectious Diseases Research in Africa (CIDRI-Africa), Faculty of Health Sciences, University of Cape Town, Rondebosch, South Africa.
    Hoppe HC; Department of Biochemistry and Microbiology, Rhodes University, Grahamstown, South Africa.; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown, South Africa.
    Legoabe LJ; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Pokaż więcej
    Źródło:
    Chemical biology & drug design [Chem Biol Drug Des] 2020 Dec; Vol. 96 (6), pp. 1387-1394. Date of Electronic Publication: 2020 Jul 26.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't
    MeSH Terms:
    Antitubercular Agents/*pharmacology
    Quinolones/*pharmacology
    Drug Screening Assays, Antitumor ; Gram-Positive Bacteria/drug effects ; HeLa Cells ; Humans ; Microbial Sensitivity Tests ; Spectrum Analysis/methods
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Synthesis and evaluation of C3 substituted chalcone-based derivatives of 7-azaindole as protein kinase inhibitors.
    Autorzy:
    Qhobosheane MA; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Legoabe LJ; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Josselin B; Sorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models Laboratory (LBI2M), Station Biologique de Roscoff, Roscoff Cedex, France.; Sorbonne Université, CNRS, FR2424, Plateforme de criblage KISSf (Kinase Inhibitor Specialized Screening facility), Station Biologique de Roscoff, Roscoff, France.
    Bach S; Sorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models Laboratory (LBI2M), Station Biologique de Roscoff, Roscoff Cedex, France.; Sorbonne Université, CNRS, FR2424, Plateforme de criblage KISSf (Kinase Inhibitor Specialized Screening facility), Station Biologique de Roscoff, Roscoff, France.
    Ruchaud S; Sorbonne Université, CNRS, UMR 8227, Integrative Biology of Marine Models Laboratory (LBI2M), Station Biologique de Roscoff, Roscoff Cedex, France.
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom, South Africa.
    Pokaż więcej
    Źródło:
    Chemical biology & drug design [Chem Biol Drug Des] 2020 Dec; Vol. 96 (6), pp. 1395-1407. Date of Electronic Publication: 2020 Aug 18.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Chalcones/*chemical synthesis
    Chalcones/*pharmacology
    Indoles/*pharmacology
    Protein Kinase Inhibitors/*chemical synthesis
    Protein Kinase Inhibitors/*pharmacology
    Antineoplastic Agents/pharmacology ; Cell Line, Tumor ; Chalcones/chemistry ; Drug Design ; Humans ; Protein Kinase Inhibitors/chemistry ; Structure-Activity Relationship
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    An Update on Development of Small-Molecule Plasmodial Kinase Inhibitors.
    Autorzy:
    Moolman C; Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom 2520, South Africa.
    Sluis RV; Focus Area for Human Metabolomics, Biochemistry, North-West University, Private Bag X6001, Potchefstroom 2520, South Africa.
    Beteck RM; Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom 2520, South Africa.
    Legoabe LJ; Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom 2520, South Africa.
    Pokaż więcej
    Źródło:
    Molecules (Basel, Switzerland) [Molecules] 2020 Nov 07; Vol. 25 (21). Date of Electronic Publication: 2020 Nov 07.
    Typ publikacji:
    Journal Article; Review
    MeSH Terms:
    Antimalarials/*pharmacology
    Drug Discovery/*trends
    Malaria/*drug therapy
    Plasmodium/*drug effects
    Protein Kinase Inhibitors/*pharmacology
    Animals ; Calcium/metabolism ; Casein Kinase I/metabolism ; Culicidae ; Drug Design ; Drug Resistance ; Glycogen Synthase Kinase 3/metabolism ; Humans ; Imidazoles/pharmacology ; Inhibitory Concentration 50 ; Life Cycle Stages/drug effects ; MAP Kinase Signaling System ; Phosphotransferases/chemistry ; Plasmodium/enzymology ; Pyridines/pharmacology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    New Quinolone-Based Thiosemicarbazones Showing Activity Against Plasmodium falciparum and Mycobacterium tuberculosis .
    Autorzy:
    Beteck RM; Division of Pharmaceutical Chemistry, Faculty of Pharmacy, Rhodes University, Grahamstown 6140, South Africa. .
    Seldon R; Drug Discovery and Development Centre (H3-D), Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa. .
    Jordaan A; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory 7925, South Africa. .
    Warner DF; SAMRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Observatory 7925, South Africa. .; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Observatory 7925, South Africa. .; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Observatory 7925, South Africa. .
    Hoppe HC; Department of Biochemistry and Microbiology, Faculty of Science, Rhodes University, Grahamstown 6140, South Africa. .; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Laming D; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Khanye SD; Division of Pharmaceutical Chemistry, Faculty of Pharmacy, Rhodes University, Grahamstown 6140, South Africa. .; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Pokaż więcej
    Źródło:
    Molecules (Basel, Switzerland) [Molecules] 2019 May 04; Vol. 24 (9). Date of Electronic Publication: 2019 May 04.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Anti-Infective Agents/*chemical synthesis
    Mycobacterium tuberculosis/*drug effects
    Plasmodium falciparum/*drug effects
    Quinolones/*chemistry
    Small Molecule Libraries/*chemical synthesis
    Thiosemicarbazones/*chemistry
    Animals ; Anti-Infective Agents/chemistry ; Anti-Infective Agents/pharmacology ; Candy ; Drug Interactions ; HeLa Cells ; Humans ; Inhibitory Concentration 50 ; Malaria, Falciparum/drug therapy ; Molecular Structure ; Small Molecule Libraries/chemistry ; Small Molecule Libraries/pharmacology ; Tuberculosis
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Cinnamoyl-Oxaborole Amides: Synthesis and Their in Vitro Biological Activity.
    Autorzy:
    Gumbo M; Faculty of Science, Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa. .
    Beteck RM; Faculty of Science, Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa. .
    Mandizvo T; Faculty of Science, Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa. .
    Seldon R; Drug Discovery and Development Centre (H3-D), Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa. .
    Warner DF; MRC/NHLS/UCT Molecular Mycobacteriology Research Unit, Department of Pathology, University of Cape Town, Rondebosch 7701, South Africa. .; Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Rondebosch 7701, South Africa. .
    Hoppe HC; Faculty of Science, Department of Biochemistry and Microbiology, Rhodes University, Grahamstown 6140, South Africa. .; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Isaacs M; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Laming D; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Tam CC; Foodborne Toxin Detection and Prevention Research Unit, Agricultural Research Service, United States Department of Agriculture, Albany, CA 94710, USA. .
    Cheng LW; Foodborne Toxin Detection and Prevention Research Unit, Agricultural Research Service, United States Department of Agriculture, Albany, CA 94710, USA. .
    Liu N; Department of Biological Sciences, University of the Pacific, Stockton, CA 95211, USA. n_.
    Land KM; Department of Biological Sciences, University of the Pacific, Stockton, CA 95211, USA. .
    Khanye SD; Faculty of Science, Department of Chemistry, Rhodes University, Grahamstown 6140, South Africa. .; Centre for Chemico- and Biomedicinal Research, Rhodes University, Grahamstown 6140, South Africa. .
    Pokaż więcej
    Źródło:
    Molecules (Basel, Switzerland) [Molecules] 2018 Aug 15; Vol. 23 (8). Date of Electronic Publication: 2018 Aug 15.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Amides/*chemical synthesis
    Anti-Infective Agents/*chemical synthesis
    Boron Compounds/*chemical synthesis
    Cinnamates/*chemical synthesis
    Amides/pharmacology ; Animals ; Anti-Infective Agents/pharmacology ; Boron Compounds/pharmacology ; Cell Survival/drug effects ; Cinnamates/pharmacology ; HeLa Cells ; Humans ; Mycobacterium tuberculosis/drug effects ; Small Molecule Libraries/chemical synthesis ; Structure-Activity Relationship ; Trichomonas vaginalis/drug effects ; Trypanocidal Agents/chemical synthesis ; Trypanocidal Agents/pharmacology ; Trypanosoma brucei brucei/drug effects ; Trypanosomiasis, African/parasitology
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Recent progress in the development of anti-malarial quinolones.
    Autorzy:
    Beteck RM
    Smit FJ
    Haynes RK
    N'Da DD; Centre of Excellence for Pharmaceutical Sciences, North-West University, Potchefstroom 2520, South Africa. .
    Pokaż więcej
    Źródło:
    Malaria journal [Malar J] 2014 Aug 30; Vol. 13, pp. 339. Date of Electronic Publication: 2014 Aug 30.
    Typ publikacji:
    Journal Article; Research Support, Non-U.S. Gov't; Review
    MeSH Terms:
    Antimalarials/*isolation & purification
    Antimalarials/*pharmacology
    Drug Discovery/*trends
    Quinolones/*isolation & purification
    Quinolones/*pharmacology
    Humans
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-10 z 10

      Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies