• Title/Summary/Keyword: Staurosporine derivative

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A Highly Selective Staurosporine Derivative Designed by a New Selectivity Filter

  • El-Deeb, Ibrahim M.;Jung, Su-Jin;Park, Byung-Sun;Yoo, Young-Jun;Choi, Ki-Hang;Yang, Young-Mok;Lee, Sang-Woo;Kim, In-Tae;Han, Dong-Keun;Lee, So-Ha
    • Bulletin of the Korean Chemical Society
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    • v.32 no.5
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    • pp.1709-1714
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    • 2011
  • KIST301135 was semi-synthetically prepared by the reaction of Staurosporine with triphosgene in anhydrous dichloromethane. The structure of KIST301135 was confirmed by $^1H$ NMR, $^{13}C$ NMR, and high resolution mass spectrum. KIST301135 was initially tested in a single dose duplicate mode at a concentration of 20 nM over a panel of 53 kinases against Staurosporine as a positive control. KIST301135 has showed inhibitions above 75% in only 2 kinases (FLT3 and JAK3 kinases) of the 53 tested kinases, while Staurosporine has showed inhibitions above 80% in about 62% of the tested kinases. KIST301135 was retested at a 5-dose testing mode over the 9 kinases inhibited by percentages over 20 at the single dose testing in order to determine its $IC_{50}$ values. KIST301135 has shown much improved kinase inhibitory selectivity relative to Staurosporine in its potency at JAK3 kinase and CAMK2b kinase.