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TitleStructure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 619-623, Year 2008
Publish dateNov 16, 2007 (structure data deposition date)
AuthorsNie, Z. / Perretta, C. / Erickson, P. / Margosiak, S. / Lu, J. / Averill, A. / Almassy, R. / Chu, S.
External linksBioorg. Med. Chem. Lett. / PubMed:18055206
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3be9:
Structure-based design and synthesis of novel macrocyclic pyrazolo[1,5-a] [1,3,5]triazine compounds as potent inhibitors of protein kinase CK2 and their anticancer activities
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-P04:
19-(cyclopropylamino)-4,6,7,15-tetrahydro-5H-16,1-(azenometheno)-10,14-(metheno)pyrazolo[4,3-o][1,3,9]triazacyclohexadecin-8(9H)-one

ChemComp-HOH:
WATER

Source
  • zea mays (maize)
KeywordsTRANSFERASE / STRUCTURE-BASED DRUG DESIGN / ENZYME-INHIBITOR COMPLEX / CASEIN KINASE II / PROTEIN KINASE CK2 / ATP-binding / Nucleotide-binding / Serine/threonine-protein kinase

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