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Identification of novel, potent and selective inhibitors of Polo-like kinase 1
- Source :
- Bioorganicmedicinal chemistry letters. 22(2)
- Publication Year :
- 2011
-
Abstract
- A series of pyrimidodiazepines was identified as potent Polo-like kinase 1 (PLK1) inhibitors. The synthesis and SAR are discussed. The lead compound 7 (RO3280) has potent inhibitory activity against PLK1, good selectivity against other kinases, and excellent in vitro cellular potency. It showed strong antitumor activity in xenograft mouse models.
- Subjects :
- Clinical Biochemistry
Pharmaceutical Science
Antineoplastic Agents
Cell Cycle Proteins
Polo-like kinase
Protein Serine-Threonine Kinases
Biochemistry
PLK1
chemistry.chemical_compound
Mice
Structure-Activity Relationship
Cell Line, Tumor
Proto-Oncogene Proteins
Drug Discovery
Potency
Structure–activity relationship
Animals
Humans
Molecular Biology
Protein Kinase Inhibitors
Cell Proliferation
Dose-Response Relationship, Drug
Molecular Structure
Kinase
Chemistry
Organic Chemistry
Stereoisomerism
Azepines
Neoplasms, Experimental
In vitro
Pyrimidines
Cell culture
Molecular Medicine
Lead compound
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 22
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....edcb14437e7b95274bb866375731eb92