Synthesis and Evaluation of Indenopyrazoles as Cyclin-Dependent Kinase Inhibitors. 3. Structure Activity Relationships at C3
- 23 October 2002
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Medicinal Chemistry
- Vol. 45 (24), 5233-5248
- https://doi.org/10.1021/jm0201722
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Prevention of Chemotherapy-Induced Alopecia in Rats by CDK InhibitorsScience, 2001
- Cyclin-dependent kinase inhibitors: novel anticancer agentsExpert Opinion on Investigational Drugs, 2000
- Arrays with Local Centers of Symmetry in Space Groups Pca21 and Pna21Acta crystallographica Section B, Structural science, crystal engineering and materials, 1998
- CYCLIN-DEPENDENT KINASES: Engines, Clocks, and MicroprocessorsAnnual Review of Cell and Developmental Biology, 1997
- Cytokinin-Derived Cyclin-Dependent Kinase Inhibitors: Synthesis and cdc2 Inhibitory Activity of Olomoucine and Related CompoundsJournal of Medicinal Chemistry, 1997
- Inhibition of Cyclin‐Dependent Kinases by Purine AnaloguesJBIC Journal of Biological Inorganic Chemistry, 1997
- Inhibition of Cyclin‐Dependent Kinases by Purine AnaloguesEuropean Journal of Biochemistry, 1994
- Purification and Crystallization of Human Cyclin-dependent Kinase 2Journal of Molecular Biology, 1993
- Growth Inhibition With Reversible Cell Cycle Arrest of Carcinoma Cells by Flavone L86-8275JNCI Journal of the National Cancer Institute, 1992
- New Colorimetric Cytotoxicity Assay for Anticancer-Drug ScreeningJNCI Journal of the National Cancer Institute, 1990