Search Results - "Muthukumar, Yazh"

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  1. 1

    Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions by Persson, Örjan, Muthukumar, Yazh, Basu, Swaraj, Jenninger, Louise, Uhler, Jay P., Berglund, Anna-Karin, McFarland, Robert, Taylor, Robert W., Gustafsson, Claes M., Larsson, Erik, Falkenberg, Maria

    Published in Nature communications (15-02-2019)
    “…Mitochondrial DNA (mtDNA) deletions are associated with mitochondrial disease, and also accumulate during normal human ageing. The mechanisms underlying mtDNA…”
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    Novel peptidomimetic compounds containing redox active chalcogens and quinones as potential anticancer agents by Shaaban, Saad, Diestel, Randi, Hinkelmann, Bettina, Muthukumar, Yazh, Verma, Rajeshwar P., Sasse, Florenz, Jacob, Claus

    Published in European journal of medicinal chemistry (01-12-2012)
    “…Many types of cancer cells are associated with a disturbed intracellular redox balance and oxidative stress (OS). Among the various agents employed to modulate…”
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  4. 4

    Cytotoxic and antivascular 1-methyl-4-(3-fluoro-4-methoxyphenyl)-5-(halophenyl)-imidazoles by Biersack, Bernhard, Muthukumar, Yazh, Schobert, Rainer, Sasse, Florenz

    Published in Bioorganic & medicinal chemistry letters (01-11-2011)
    “…A series of 1-methyl-4,5-diphenylimidazoles 6 with various patterns of m-halogen substitution at the 5-phenyl ring were tested for cytotoxicity in cancer and…”
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    An Improved Route to (+)-Tedanolide and Analysis of Its Subtle Effects Controlling Conformation and Biological Behaviour by Diaz, Nina, Zhu, Mingzhao, Ehrlich, Gunnar, Eggert, Ulrike, Muthukumar, Yazh, Sasse, Florenz, Kalesse, Markus

    Published in Chemistry : a European journal (16-04-2012)
    “…The improved synthesis of the antitumor compound (+)‐tedanolide is described through an aldol coupling of bis‐ketone 7. This modification shortens the…”
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    The Marine Polyketide Myriaporone 3/4 Stalls Translation by Targeting the Elongation Phase by Muthukumar, Yazh, Roy, Myriam, Raja, Aruna, Taylor, Richard E., Sasse, Florenz

    “…Myriaporone 3/4, a cytotoxic polyketide, has been reported as an inhibitor of eukaryotic protein synthesis. However, the mechanism by which it inhibits…”
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  7. 7

    The Synthesis and Biological Evaluation of Desepoxyisotedanolide and a Comparison with Desepoxytedanolide by Naini, Arun, Muthukumar, Yazh, Raja, Aruna, Franke, Raimo, Harrier, Ian, Smith III, Amos B., Lee, Dongjoo, Taylor, Richard E., Sasse, Florenz, Kalesse, Markus

    Published in Angewandte Chemie International Edition (01-06-2015)
    “…The tedanolides are biologically active polyketides that exhibit a macrolactone constructed from a primary alcohol. Since polyketidal transformations only…”
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  8. 8

    Synthesis of Simplified Tedanolide Analogues-Connecting Tedanolide to Myriaporone and Gephyronic Acid by Diaz, Nina, Naini, Arun, Muthukumar, Yazh, Sasse, Florenz, Kalesse, Markus

    Published in ChemMedChem (01-05-2012)
    “…Southern belles! Simplified analogues of tedanolide, a natural product with picomolar activity against a range of tumor cell lines, were synthesized and…”
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    Die Synthese und biologische Validierung von Desepoxyisotedanolid und dessen Vergleich mit Desepoxytedanolid by Naini, Arun, Muthukumar, Yazh, Raja, Aruna, Franke, Raimo, Harrier, Ian, Smith, Amos B., Lee, Dongjoo, Taylor, Richard E., Sasse, Florenz, Kalesse, Markus

    Published in Angewandte Chemie (01-06-2015)
    “…Die Tedanolide sind biologisch aktive Polyketide, deren Makrolaktonring aus einem primären Alkohol aufgebaut ist. Da Polyketidumwandlungen nur sekundäre…”
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  12. 12

    Die Synthese und biologische Validierung von Desepoxyisotedanolid und dessen Vergleich mit Desepoxytedanolid by Naini, Arun, Muthukumar, Yazh, Raja, Aruna, Franke, Raimo, Harrier, Ian, Smith III, Amos B., Lee, Dongjoo, Taylor, Richard E., Sasse, Florenz, Kalesse, Markus

    Published in Angewandte Chemie (01-06-2015)
    “…Abstract Die Tedanolide sind biologisch aktive Polyketide, deren Makrolaktonring aus einem primären Alkohol aufgebaut ist. Da Polyketidumwandlungen nur…”
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