Structure-activity relationship study of 4-(thiazol-5-yl)benzoic acid derivatives as potent protein kinase CK2 inhibitors.

نویسندگان

  • Hiroaki Ohno
  • Daiki Minamiguchi
  • Shinya Nakamura
  • Keito Shu
  • Shiho Okazaki
  • Maho Honda
  • Ryosuke Misu
  • Hirotomo Moriwaki
  • Shinsuke Nakanishi
  • Shinya Oishi
  • Takayoshi Kinoshita
  • Isao Nakanishi
  • Nobutaka Fujii
چکیده

Two classes of modified analogs of 4-(thiazol-5-yl)benzoic acid-type CK2 inhibitors were designed. The azabenzene analogs, pyridine- and pyridazine-carboxylic acid derivatives, showed potent protein kinase CK2 inhibitory activities [IC50 (CK2α)=0.014-0.017μM; IC50 (CK2α')=0.0046-0.010μM]. Introduction of a 2-halo- or 2-methoxy-benzyloxy group at the 3-position of the benzoic acid moiety maintained the potent CK2 inhibitory activities [IC50 (CK2α)=0.014-0.016μM; IC50 (CK2α')=0.0088-0.014μM] and led to antiproliferative activities [CC50 (A549)=1.5-3.3μM] three to six times higher than those of the parent compound.

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عنوان ژورنال:
  • Bioorganic & medicinal chemistry

دوره 24 5  شماره 

صفحات  -

تاریخ انتشار 2016