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10.1021/ml3004632

http://scihub22266oqcxt.onion/10.1021/ml3004632
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C4027554!4027554!24900662
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suck abstract from ncbi


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pmid24900662      ACS+Med+Chem+Lett 2013 ; 4 (2): 297-301
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  • Discovery of Indenopyrazoles as a New Class of Hypoxia Inducible Factor (HIF)-1 Inhibitors #MMPMID24900662
  • Minegishi H; Fukashiro S; Ban HS; Nakamura H
  • ACS Med Chem Lett 2013[Feb]; 4 (2): 297-301 PMID24900662show ga
  • The indenopyrazole framework was investigated as a new class of HIF-1? inhibitors. Indenopyrazole 2l was found to most strongly inhibit the hypoxia-induced HIF-1? transcriptional activity (IC50 = 0.014 ?M) among all of the known compounds having relatively simple structures, unlike manassantins. Indenopyrazole 2l suppressed HIF-1? transcriptional activity without affecting both HIF-1? protein accumulation and HIF-1?/HIF-1? heterodimerization in nuclei under the hypoxic conditions, suggesting that 2l probably affected the transcriptional pathway induced by the HIF-1?/HIF-1? heterodimer.
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