Title : Discovery and initial characterization of the paullones, a novel class of small-molecule inhibitors of cyclin-dependent kinases.

Pub. Date : 1999 Jun 1

PMID : 10363974






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 9-Bromo-7,12-dihydro-indolo[3,2-d][1]benzazepin-6(5H)-one, NSC-664704 (kenpaullone), is reported here to be a potent inhibitor of CDK1/cyclin B (IC50, 0.4 microM). kenpaullone cyclin dependent kinase 1 Homo sapiens
2 9-Bromo-7,12-dihydro-indolo[3,2-d][1]benzazepin-6(5H)-one, NSC-664704 (kenpaullone), is reported here to be a potent inhibitor of CDK1/cyclin B (IC50, 0.4 microM). kenpaullone cyclin dependent kinase 1 Homo sapiens
3 Analogues of kenpaullone, in particular 10-bromopaullone (NSC-672234), also inhibited various protein kinases including CDKs. kenpaullone cyclin dependent kinase 1 Homo sapiens
4 Kenpaullone represents a novel chemotype for compounds that preferentially inhibit CDKs. kenpaullone cyclin dependent kinase 1 Homo sapiens