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  1. Buch: Modern alkaloids

    Fattorusso, Ernesto

    structure, isolation, synthesis and biology

    2008  

    Verfasserangabe ed. by Ernesto Fattorusso
    Schlagwörter Alkaloide
    Schlagwörter Pflanzenalkaloide
    Sprache Englisch
    Umfang XXIV, 665 S. : Ill., graph. Darst.
    Verlag Wiley-VCH
    Erscheinungsort Weinheim
    Erscheinungsland Deutschland
    Dokumenttyp Buch
    HBZ-ID HT015337311
    ISBN 978-3-527-31521-5 ; 3-527-31521-7
    Datenquelle Katalog ZB MED Medizin, Gesundheit

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  2. Buch ; Online: Handbook of marine natural products

    Fattorusso, Ernesto

    (Springer reference)

    2012  

    Verfasserangabe Ernesto Fattorusso ... ed
    Serientitel Springer reference
    Schlagwörter Aquatic biology ; Biochemistry ; Chemistry, Organic ; Life sciences ; Oceanography ; Pharmacy ; Toxicology
    Sprache Englisch
    Umfang Online-Ressource (xxiv, 1452 p)
    Verlag Springer
    Erscheinungsort Dordrecht ;London
    Dokumenttyp Buch ; Online
    Anmerkung Includes bibliographical references and index
    ISBN 9789048138333 ; 9789048138340 ; 9048138337 ; 9048138345
    DOI 10.1007/978-90-481-3834-0
    Datenquelle Ehemaliges Sondersammelgebiet Küsten- und Hochseefischerei

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  3. Buch: Modern alkaloids

    Fattorusso, Ernesto

    structure, isolation, synthesis and biology

    2008  

    Verfasserangabe ed. by Ernesto Fattorusso and Orazio Taglialatela-Scafati
    Schlagwörter Alkaloids ; Alkaloids/Structure ; Alkaloide
    Sprache Englisch
    Umfang XXIV, 665 S, Ill., graph. Darst, 240 mm x 170 mm
    Verlag WILEY-VCH
    Erscheinungsort Weinheim
    Dokumenttyp Buch
    Anmerkung Literaturangaben
    ISBN 3527315217 ; 9783527315215
    Datenquelle Katalog der Technische Informationsbibliothek Hannover

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  4. Buch: Modern alkaloids

    Fattorusso, Ernesto

    structure, isolation, synthesis and biology

    2008  

    Verfasserangabe ed. by Ernesto Fattorusso and Orazio Taglialatela-Scafati
    Schlagwörter Alkaloids ; Alkaloids/Structure ; Alkaloide
    Sprache Englisch
    Umfang XXIV, 665 S, Ill., graph. Darst, 240 mm x 170 mm
    Verlag WILEY-VCH
    Erscheinungsort Weinheim
    Dokumenttyp Buch
    Anmerkung Literaturangaben
    ISBN 3527315217 ; 9783527315215
    Datenquelle Bundesinstitut für Risikobewertung

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  5. Buch: Modern alkaloids

    Fattorusso, Ernesto

    structure, isolation, synthesis and biology

    2008  

    Verfasserangabe ed. by Ernesto Fattorusso and Orazio Taglialatela-Scafati
    Schlagwörter Alkaloids ; Alkaloids/Structure ; Alkaloide
    Sprache Englisch
    Umfang XXIV, 665 S, Ill., graph. Darst, 240 mm x 170 mm
    Dokumenttyp Buch
    Anmerkung Literaturangaben
    ISBN 3527315217 ; 9783527315215
    Datenquelle Leibniz-Institut für Pflanzenbiochemie

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  6. Artikel: Thorexanthin, a New Carotenoid Pigment from the Caribbean Sponge Thorecta horridus

    Fattorusso, Ernesto / Virginia Lanzotti / Silvana Magno / Luciano Mayol

    Zeitschrift für Naturforschung. 2014 June 2, v. 47, no. 10

    2014  

    Abstract: The red-pigmented caribbean sponge Thorecta horridus contains thorexanthin (3-methoxy-β-X-caroten-4-one) as a new carotenoid pigment. Its structure was determined by spectroscopic methods, including 2 D NMR experiments. ...

    Abstract The red-pigmented caribbean sponge Thorecta horridus contains thorexanthin (3-methoxy-β-X-caroten-4-one) as a new carotenoid pigment. Its structure was determined by spectroscopic methods, including 2 D NMR experiments.
    Schlagwörter carotenoids ; nuclear magnetic resonance spectroscopy ; Caribbean
    Sprache Englisch
    Erscheinungsverlauf 2014-0602
    Umfang p. 1477-1479.
    Erscheinungsort Verlag der Zeitschrift für Naturforschung
    Dokumenttyp Artikel
    ZDB-ID 124635-5
    ISSN 0340-5087 ; 0044-3174 ; 0932-0776 ; 0341-0447 ; 0341-0420
    ISSN 0340-5087 ; 0044-3174 ; 0932-0776 ; 0341-0447 ; 0341-0420
    DOI 10.1515/znb-1992-1020
    Datenquelle NAL Katalog (AGRICOLA)

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  7. Artikel ; Online: The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism.

    Persico, Marco / Fattorusso, Roberto / Taglialatela-Scafati, Orazio / Chianese, Giuseppina / de Paola, Ivan / Zaccaro, Laura / Rondinelli, Francesca / Lombardo, Marco / Quintavalla, Arianna / Trombini, Claudio / Fattorusso, Ernesto / Fattorusso, Caterina / Farina, Biancamaria

    Scientific reports

    2017  Band 7, Seite(n) 45485

    Abstract: In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce ... ...

    Abstract In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species after being reductively activated by heme. In particular, similarly to artemisinin, the formation of radicals prone to inter-molecular reactions should represent the key event responsible for Plasmodium death. To our knowledge this is the first experimental investigation on the reductive activation of simple antimalarial endoperoxides (1,2-dioxanes) by heme and results were compared to the ones previously obtained from the reaction with FeCl
    Mesh-Begriff(e) Antimalarials/chemistry ; Antimalarials/metabolism ; Binding Sites ; Dioxanes/chemistry ; Dioxanes/metabolism ; Dioxanes/pharmacology ; Ferrous Compounds/chemistry ; Ferrous Compounds/metabolism ; Heme/chemistry ; Heme/metabolism ; Magnetic Resonance Spectroscopy ; Mass Spectrometry ; Molecular Conformation ; Molecular Docking Simulation
    Chemische Substanzen Antimalarials ; Dioxanes ; Ferrous Compounds ; Heme (42VZT0U6YR) ; ferrous chloride (S3Y25PHP1W)
    Sprache Englisch
    Erscheinungsdatum 2017-04-06
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep45485
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  8. Artikel ; Online: Marine antimalarials.

    Fattorusso, Ernesto / Taglialatela-Scafati, Orazio

    Marine drugs

    2009  Band 7, Heft 2, Seite(n) 130–152

    Abstract: Malaria is an infectious disease causing at least 1 million deaths per year, and, unfortunately, the chemical entities available to treat malaria are still too limited. In this review we highlight the contribution of marine chemistry in the field of ... ...

    Abstract Malaria is an infectious disease causing at least 1 million deaths per year, and, unfortunately, the chemical entities available to treat malaria are still too limited. In this review we highlight the contribution of marine chemistry in the field of antimalarial research by reporting the most important results obtained until the beginning of 2009, with particular emphasis on recent discoveries. About 60 secondary metabolites produced by marine organisms have been grouped into three structural types and discussed in terms of their reported antimalarial activities. The major groups of metabolites include isonitrile derivatives, alkaloids and endoperoxide derivatives. The following discussion evidences that antimalarial marine molecules can efficiently integrate the panel of lead compounds isolated from terrestrial sources with new chemical backbones and, sometimes, with unique functional groups.
    Mesh-Begriff(e) Alkaloids/chemistry ; Alkaloids/pharmacology ; Animals ; Antimalarials/chemistry ; Antimalarials/pharmacology ; Cyanobacteria/chemistry ; Diterpenes/chemistry ; Diterpenes/pharmacology ; Marine Biology ; Nitriles/chemistry ; Nitriles/pharmacology ; Peroxides/chemistry ; Peroxides/pharmacology ; Plasmodium/drug effects ; Porifera/chemistry
    Chemische Substanzen Alkaloids ; Antimalarials ; Diterpenes ; Nitriles ; Peroxides
    Sprache Englisch
    Erscheinungsdatum 2009-04-23
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article ; Review
    ZDB-ID 2175190-0
    ISSN 1660-3397 ; 1660-3397
    ISSN (online) 1660-3397
    ISSN 1660-3397
    DOI 10.3390/md7020130
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Marine endoperoxides as antimalarial lead compounds

    Fattorusso, Ernesto / Taglialatela-Scafati, Orazio

    Phytochemistry reviews proceedings of the Phytochemical Society of Europe. 2010 Dec., v. 9, no. 4

    2010  

    Abstract: Malaria, a pathology caused by protozoa belonging to the genus Plasmodium, is one of the major threats to global health, with about 300-500 million new clinical cases occurring every year and 1-3 million annual deaths. The recrudescence in the number of ... ...

    Abstract Malaria, a pathology caused by protozoa belonging to the genus Plasmodium, is one of the major threats to global health, with about 300-500 million new clinical cases occurring every year and 1-3 million annual deaths. The recrudescence in the number of fatal cases registered in recent years can be attributed to the diffusion of multi-drug resistant strains of Plasmodium, which make less effective the limited armamentarium of available drugs. Living organisms are a recognized source of potentially bioactive molecules and, among them, marine natural products are emerging as one of the most interesting sources to be exploited for the discovery of new antimalarial compounds. In this article we will report results obtained for a single class of marine metabolites, namely endoperoxide-containing derivatives. Many of these molecules possess a simple six-membered 1,2-dioxygenated ring bearing two or three alkyl/aryl groups of different complexity. They can be divided according to the group linked at one of the two endoperoxide-oxygen bearing carbons: peroxyketal derivatives (methoxy group) or non-peroxyketal derivatives (methyl/ethyl groups). Molecules belonging to these classes show in vitro antimalarial activity in the nanomolar range on chloroquine-resistant strains. A number of investigations gave insights into the mechanism of action of these molecules, suggesting structural changes to optimize their antimalarial activity.
    Schlagwörter malaria ; artemisinin ; peroxides
    Sprache Englisch
    Erscheinungsverlauf 2010-12
    Umfang p. 515-524.
    Verlag Springer Netherlands
    Erscheinungsort Dordrecht
    Dokumenttyp Artikel
    ZDB-ID 2065661-0
    ISSN 1572-980X ; 1568-7767
    ISSN (online) 1572-980X
    ISSN 1568-7767
    DOI 10.1007/s11101-010-9197-6
    Datenquelle NAL Katalog (AGRICOLA)

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  10. Buch: Modern alkaloids

    Fattorusso, Ernesto / Taglialatela-Scafati, Orazio

    structure, isolation, synthesis and biology

    2008  

    Verfasserangabe edited by Ernesto Fattorusso and Orazio Taglialatela-Scafati
    Schlagwörter Alkaloids. ; Alkaloids/Structure.
    Sprache Englisch
    Umfang xxiv, 665 p. :, ill. ;, 25 cm.
    Verlag Wiley-VCH
    Erscheinungsort Weinheim ; Chichester
    Dokumenttyp Buch
    ISBN 9783527315215 ; 3527315217
    Datenquelle NAL Katalog (AGRICOLA)

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