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TitleSynthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 3. Structure Activity Relationships at C3
Journal, issue, pagesJ. Med. Chem., Vol. 45, Page 5233-5248, Year 2002
Publish dateSep 27, 2005 (structure data deposition date)
AuthorsYue, E.W. / Higley, C.A. / Dimeo, S.V. / Carini, D.J. / Nugiel, D.A. / Benware, C. / Benfield, P.A. / Cox, S. / Burton, C.R. / Grafstrom, R.H. ...Yue, E.W. / Higley, C.A. / Dimeo, S.V. / Carini, D.J. / Nugiel, D.A. / Benware, C. / Benfield, P.A. / Cox, S. / Burton, C.R. / Grafstrom, R.H. / Sharp, D.M. / Sisk, L.M. / Boylan, J.F. / Muckelbauer, J.K. / Smallwood, A.M. / Chen, H. / Chang, C.-H. / Seitz, S.P. / Trainor, G.L.
External linksJ. Med. Chem. / PubMed:12431051
MethodsX-ray diffraction
Resolution1.85 Å
Structure data

PDB-2b55:
Human cyclin dependent kinase 2 (cdk2) complexed with indenopyraxole DIN-101312
Method: X-RAY DIFFRACTION / Resolution: 1.85 Å

Chemicals

ChemComp-D31:
2-(4-(AMINOMETHYL)PIPERIDIN-1-YL)-N-(3_CYCLOHEXYL-4-OXO-2,4-DIHYDROINDENO[1,2-C]PYRAZOL-5-YL)ACETAMIDE

ChemComp-HOH:
WATER

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

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