Discovery of a Novel Family of CDK Inhibitors with the Program LIDAEUS
- 1 April 2003
- Vol. 11 (4) , 399-410
- https://doi.org/10.1016/s0969-2126(03)00060-1
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Specificity and mechanism of action of some commonly used protein kinase inhibitorsBiochemical Journal, 2000
- Structural Mechanism for STI-571 Inhibition of Abelson Tyrosine KinaseScience, 2000
- Mechanisms of cyclin-dependent kinase regulation: structures of cdks, their cyclin activators, and cip and INK4 inhibitorsJournal of Molecular Biology, 1999
- An example of a protein ligand found by database mining: description of the docking method and its verification by a 2.3 Å X-ray structure of a Thrombin-Ligand complexJournal of Molecular Biology, 1998
- Refinement of Macromolecular Structures by the Maximum-Likelihood MethodActa Crystallographica Section D-Biological Crystallography, 1997
- [20] Processing of X-ray diffraction data collected in oscillation modePublished by Elsevier ,1997
- X-SITE: Use of Empirically Derived Atomic Packing Preferences to Identify Favourable Interaction Regions in the Binding Sites of ProteinsJournal of Molecular Biology, 1996
- Phenylamino‐Pyrimidine (PAP) Derivatives: A New Class of Potent and Selective Inhibitors of Protein Kinase C (PKC)Archiv der Pharmazie, 1996
- Purification and Crystallization of Human Cyclin-dependent Kinase 2Journal of Molecular Biology, 1993
- Säureamid‐Reaktionen, XLV. Untersuchungen über die Reaktionsfähigkeit von Formamidinen, Dimethylformamid‐diäthylacetal (Amidacetal) und Bis‐dimethyl‐amino‐methoxy‐methan (Aminalester)European Journal of Inorganic Chemistry, 1964