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TitleSynthesis and SAR studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off-target kinase selectivity.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 22, Page 3544-3549, Year 2012
Publish dateDec 29, 2011 (structure data deposition date)
AuthorsVoss, M.E. / Rainka, M.P. / Fleming, M. / Peterson, L.H. / Belanger, D.B. / Siddiqui, M.A. / Hruza, A. / Voigt, J. / Gray, K. / Basso, A.D.
External linksBioorg. Med. Chem. Lett. / PubMed:22503250
MethodsX-ray diffraction
Resolution2.66 Å
Structure data

PDB-3vap:
Synthesis and SAR Studies of imidazo-[1,2-a]-pyrazine Aurora kinase inhibitors with improved off target kinase selectivity
Method: X-RAY DIFFRACTION / Resolution: 2.66 Å

Chemicals

ChemComp-0FY:
3-(1-{2-[(3-fluoropyridinium-4-yl)amino]-2-oxoethyl}-1H-pyrazol-4-yl)-6-methyl-8-[(3-{[(1R,3R)-3-methylpiperidinium-1-yl]methyl}-1,2-thiazol-5-yl)amino]imidazo[1,2-a]pyrazin-1-ium

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / kinase / cell cycle / inhibitor / transferase / TRANSFERASE-TRANSFERASE INHIBITOR complex

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