Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase.
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Structure of human Bloom's syndrome helicase in complex with ADP and duplex DNARECQL1 and WRN DNA repair helicases: potential therapeutic targets and proliferative markers against cancers.Targeting the homologous recombination pathway by small molecule modulatorsA Platform to Enable the Pharmacological Profiling of Small Molecules in Gel-Based Electrophoretic Mobility Shift Assays.Targeting homologous recombination-mediated DNA repair in cancer.BRCA2 and RAD51 promote double-strand break formation and cell death in response to gemcitabine.RECQ1 expression is upregulated in response to DNA damage and in a p53-dependent manner.Small-Molecule Inhibitors Targeting DNA Repair and DNA Repair Deficiency in Research and Cancer Therapy.New Insights Into DNA Helicases as Druggable Targets for Cancer Therapy
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Synthesis and SAR studies of 5-(pyridin-4-yl)-1,3,4-thiadiazol-2-amine derivatives as potent inhibitors of Bloom helicase.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 13 August 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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type
label
Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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prefLabel
Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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P2860
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P1476
Synthesis and SAR studies of 5 ...... inhibitors of Bloom helicase.
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Andrew S Rosenthal
David J Maloney
Giang H Nguyen
Ian D Hickson
Thomas S Dexheimer
Wai Kit Chu
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10.1016/J.BMCL.2013.08.025
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P577
2013-08-13T00:00:00Z