Search Results - "Lough, Rachel"
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Rationally Designed High-Affinity 2-Amino-6-halopurine Heat Shock Protein 90 Inhibitors That Exhibit Potent Antitumor Activity
Published in Journal of medicinal chemistry (14-06-2007)“…Heat shock protein 90 (Hsp90) is a molecular chaperone protein implicated in stabilizing the conformation and maintaining the function of many cell-signaling…”
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7‘-Substituted Benzothiazolothio- and Pyridinothiazolothio-Purines as Potent Heat Shock Protein 90 Inhibitors
Published in Journal of medicinal chemistry (24-08-2006)“…We report on the discovery of benzo- and pyridino- thiazolothiopurines as potent heat shock protein 90 inhibitors. The benzothiazole moiety is exceptionally…”
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Orally Active Purine-Based Inhibitors of the Heat Shock Protein 90
Published in Journal of medicinal chemistry (26-01-2006)“…Orally active Hsp90 inhibitors are of interest as potential chemotherapeutic agents. Recently, fully synthetic 8-benzyladenines and 8-sulfanyladenines such as…”
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The topoisomerase II–Hsp90 complex: A new chemotherapeutic target?
Published in International journal of cancer (01-06-2006)“…The modulation of DNA topology by topoisomerase II plays a crucial role during chromosome condensation and segregation in mitosis and has thus become a highly…”
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BIIB021, a synthetic Hsp90 inhibitor, has broad application against tumors with acquired multidrug resistance
Published in International journal of cancer (01-03-2010)“…17‐AAG, the first‐generation clinical Hsp90 inhibitor, exhibits promising antitumor activity in clinical studies, but is limited by poor solubility and…”
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EC144 Is a Potent Inhibitor of the Heat Shock Protein 90
Published in Journal of medicinal chemistry (13-09-2012)“…Alkyne 40, 5-(2-amino-4-chloro-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2-methylpent-4-yn-2-ol (EC144), is a second…”
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Synthesis and Biological Evaluation of a New Class of Geldanamycin Derivatives as Potent Inhibitors of Hsp90
Published in Journal of medicinal chemistry (15-07-2004)“…The heat shock protein Hsp90 has increasingly become an important therapeutic target especially for treatment of cancers. Inhibition of the ATPase activity of…”
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