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TitleSynthesis and biological evaluation of 1-aryl-4,5-dihydro-1h-pyraxolo[3,4-d]pyrimidin-4-one inhibitors of cyclin dependent kinases
Journal, issue, pagesJ. Med. Chem., Vol. 47, Page 5894-5911, Year 2004
Publish dateSep 27, 2005 (structure data deposition date)
AuthorsMarkwalder, J.A. / Arnone, M.R. / Benfield, P.A. / Boisclair, M. / Burton, C.R. / Chang, C.-C. / Cox, S.S. / Czerniak, P.M. / Dean, C.L. / Dolenaik, D. ...Markwalder, J.A. / Arnone, M.R. / Benfield, P.A. / Boisclair, M. / Burton, C.R. / Chang, C.-C. / Cox, S.S. / Czerniak, P.M. / Dean, C.L. / Dolenaik, D. / Grafstrom, R. / Harrison, B.A. / Kaltenbach III, R.F. / Nugiel, D.A. / Rossi, K.A. / Sherk, S.R. / Sisk, L.M. / Stouten, P. / Trainor, G.L. / Worland, P. / Seitz, S.P.
External linksJ. Med. Chem. / PubMed:15537345
MethodsX-ray diffraction
Resolution1.85 Å
Structure data

PDB-2b54:
Human cyclin dependent kinase 2 (CKD2)complexed with DIN-232305
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

Chemicals

ChemComp-D05:
6-(3,4-DIHYDROXYBENZYL)-3-ETHYL-1-(2,4,6-TRICHLOROPHENYL)-1H-PYRAZOLO[3,4-D]PYRIMIDIN-4(5H)-ONE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / PROTEIN KINASE / CELL CYCLE / PHOSPHORYLATION / CELL DIVISION / MITOSIS / INHIBITION

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