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Title4-(Aminoalkylamino)-3-benzimidazole-quinolinones as potent CHK-1 inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 16, Page 3121-3124, Year 2006
Publish dateMar 16, 2006 (structure data deposition date)
AuthorsNi, Z.J. / Barsanti, P. / Brammeier, N. / Diebes, A. / Poon, D.J. / Ng, S. / Pecchi, S. / Pfister, K. / Renhowe, P.A. / Ramurthy, S. ...Ni, Z.J. / Barsanti, P. / Brammeier, N. / Diebes, A. / Poon, D.J. / Ng, S. / Pecchi, S. / Pfister, K. / Renhowe, P.A. / Ramurthy, S. / Wagman, A.S. / Bussiere, D.E. / Le, V. / Zhou, Y. / Jansen, J.M. / Ma, S. / Gesner, T.G.
External linksBioorg. Med. Chem. Lett. / PubMed:16603354
MethodsX-ray diffraction
Resolution3 Å
Structure data

PDB-2gdo:
4-(Aminoalkylamino)-3-Benzimidazole-Quinolinones As Potent CHK1 Inhibitors
Method: X-RAY DIFFRACTION / Resolution: 3 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-12C:
4-[(3S)-1-AZABICYCLO[2.2.2]OCT-3-YLAMINO]-3-(1H-BENZIMIDAZOL-2-YL)-6-CHLOROQUINOLIN-2(1H)-ONE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / DRUG DESIGN / ATP-BINDING / CELL CYCLE / DNA DAMAGE / SERINE/THREONINE-PROTEIN KINASE

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