Search Results - "Pürstinger, Gerhard"

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    Identification of 2‑(4-(Phenylsulfonyl)piperazine-1-yl)pyrimidine Analogues as Novel Inhibitors of Chikungunya Virus by Moesslacher, Julia, Battisti, Verena, Delang, Leen, Neyts, Johan, Abdelnabi, Rana, Pürstinger, Gerhard, Urban, Ernst, Langer, Thierry

    Published in ACS medicinal chemistry letters (14-05-2020)
    “…The chikungunya virus (CHIKV) is a mosquito-transmitted alphavirus, and it is the causative agent of chikungunya fever (CHIKF). Although it has re-emerged as…”
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    Allosteric Regulation of Phosphatidylinositol 4‑Kinase III Beta by an Antipicornavirus Compound MDL-860 by Arita, Minetaro, Dobrikov, Georgi, Pürstinger, Gerhard, Galabov, Angel S

    Published in ACS infectious diseases (11-08-2017)
    “…MDL-860 is a broad-spectrum antipicornavirus compound discovered in 1982 and one of the few promising candidates effective in in vivo virus infection. Despite…”
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    Potential use of antiviral agents in polio eradication by De Palma, Armando M, Pürstinger, Gerhard, Wimmer, Eva, Patick, Amy K, Andries, Koen, Rombaut, Bart, De Clercq, Erik, Neyts, Johan

    Published in Emerging infectious diseases (01-04-2008)
    “…In 1988, the World Health Assembly launched the Global Polio Eradication Initiative, which aimed to use large-scale vaccination with the oral vaccine to…”
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    Anti-enteroviral triple combination of viral replication inhibitors: activity against coxsackievirus B1 neuroinfection in mice by Stoyanova, Adelina, Nikolova, Ivanka, Pürstinger, Gerhard, Dobrikov, Georgi, Dimitrov, Vladimir, Philipov, Stefan, Galabov, Angel S

    Published in Antiviral chemistry & chemotherapy (01-12-2015)
    “…Background Chemotherapy is an important tool for controlling enterovirus infections, but clinically effective anti-enterovirus drugs do not currently exist,…”
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    Synthesis, Cytotoxic, and Antitumor Activities of 2-Pyridylhydrazones Derived from 3-Benzoylpyridazines by Easmon, Johnny, Pürstinger, Gerhard, Heinisch, Gottfried, Fiebig, Hans H., Roth, Thomas, Hofmann, Johann

    Published in Archiv der Pharmazie (Weinheim) (01-08-2014)
    “…A series of 2‐pyridylhydrazones derived from phenyl‐pyridazin‐3‐yl‐methanones were prepared in search for potential novel antitumor agents. The stereochemistry…”
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    Synthesis, Structure−Activity Relationships, and Antitumor Studies of 2-Benzoxazolyl Hydrazones Derived from Alpha-(N)-acyl Heteroaromatics by Easmon, Johnny, Pürstinger, Gerhard, Thies, Katrin-Sofia, Heinisch, Gottfried, Hofmann, Johann

    Published in Journal of medicinal chemistry (19-10-2006)
    “…Recently we have described the antitumor activities of 2-benzoxazolylhydrazones derived from 2-formyl and 2-acetylpyridines. In search of a more efficacious…”
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    Synthesis and anti-CVB 3 evaluation of substituted 5-nitro-2-phenoxybenzonitriles by Pürstinger, Gerhard, De Palma, Armando M., Zimmerhofer, Günther, Huber, Simone, Ladurner, Sophie, Neyts, Johan

    Published in Bioorganic & medicinal chemistry (15-09-2008)
    “…The synthesis and SAR of a series of 60 substituted 2-phenoxy-5-nitrobenzonitriles (analogues of MDL-860) as inhibitors of enterovirus replication (in…”
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    Coxsackievirus mutants that can bypass host factor PI4KIIIβ and the need for high levels of PI4P lipids for replication by van der Schaar, Hilde M, van der Linden, Lonneke, Lanke, Kjerstin H W, Strating, Jeroen R P M, Pürstinger, Gerhard, de Vries, Erik, de Haan, Cornelis A M, Neyts, Johan, van Kuppeveld, Frank J M

    Published in Cell research (01-11-2012)
    “…RNA viruses can rapidly mutate and acquire resistance to drugs that directly target viral enzymes, which poses serious problems in a clinical context…”
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    Foreign Direct Investments and Mergers and Acquisitions in Slovakia by Pürstinger, Gerhard, Soltés, Vincent

    Published in Theory, methodology, practice (01-02-2007)
    “…The paper gives answer why Slovakia is so attractive for Foreign Direct Investments. There are discussed economics factors in Slovakia and there are compared…”
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    Substituted imidazopyridines as potent inhibitors of HCV replication by Vliegen, Inge, Paeshuyse, Jan, De Burghgraeve, Tine, Lehman, Laura S, Paulson, Matthew, Shih, I-Hung, Mabery, Eric, Boddeker, Nina, De Clercq, Erik, Reiser, Hans, Oare, David, Lee, William A, Zhong, Weidong, Bondy, Steven, Pürstinger, Gerhard, Neyts, Johan

    Published in Journal of hepatology (01-05-2009)
    “…Background/Aims Following lead optimization, a set of substituted imidazopyridines was identified as potent and selective inhibitors of in vitro HCV…”
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    H1PVAT is a novel and potent early-stage inhibitor of poliovirus replication that targets VP1 by TIJSMA, Aloys, THIBAUT, Hendrik Jan, MARCHAND, Arnaud, CHALTIN, Patrick, NEYTS, Johan, LEYSSEN, Pieter, SPIESER, Stéphane A. H, DE PALMA, Armando, KOUKNI, Mohamed, RHODEN, Eric, OBERSTE, Steve, PÜRSTINGER, Gerhard, VOLNY-LURAGHI, Antonia, MARTIN, Javier

    Published in Antiviral research (01-10-2014)
    “…A novel small molecule, H1PVAT, was identified as a potent and selective inhibitor of the in vitro replication of all three poliovirus serotypes, whereas no…”
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