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Volumn 19, Issue 11, 2009, Pages 3019-3022

Structure-based design of 3-aryl-6-amino-triazolo[4,3-b]pyridazine inhibitors of Pim-1 kinase

Author keywords

Permeability; Pim 1 kinase; Pim 1 kinase inhibitors; Solubility; Triazolo 4,3 b pyridazine

Indexed keywords

3 6 AMINO TRIAZOLO[4,3 B]PYRIDAZINE INHIBITOR; ADENOSINE TRIPHOSPHATE; PROTEIN KINASE PIM 1; PYRIDAZINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 65149094214     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.04.061     Document Type: Article
Times cited : (55)

References (24)
  • 21
    • 0031793432 scopus 로고    scopus 로고
    • note
    • 2, 25 mM NaCl, 1 mM DTT, 20 μg/ml BSA and 1.5% DMSO. Final substrate concentrations in the assay were 120 μM ATP and 200 μM peptide (RRRLSSLRA). Assays were carried out at 30 °C. using 50 nM PIM-1. Final concentrations of the components of the coupled enzyme system were 2.5 mM phosphoenolpyruvate, 350 μM NADH, 30 μg/ml pyruvate kinase and 10 μg/ml lactate dehydrogenase.
  • 23
    • 65149105003 scopus 로고    scopus 로고
    • note
    • Solubility at pH 7.4 was determined by addition of 49 μL of 10 mM DPBS phosphate buffer to 1 μL of 10 mM DMSO solution. The solution is mixed overnight and concentration determined by HPLC.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.