Olomoucine
Discontinued Product
Chemical Name: 6-(Benzylamino)-2-(2-hydroxyethylamino)-9-methylpurine
Biological Activity
ATP-competitive cyclin-dependent kinase (cdk) inhibitor (reported IC50 values are 0.6 and 0.94 - 8 μM for cdk7 and cdk2 respectively, and >1 μM for cdk1 and cdk9. Induces cell cycle arrest at G1 in human fibroblasts.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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High-throughput genotoxicity assay identifies antioxidants as inducers of DNA damage response and cell death.
Fox JT, Sakamuru S, Huang R
Proc. Natl. Acad. Sci. U.S.A., 2012;109(14):5423-8. -
How selective are pharmacological inhibitors of cell-cycle-regulating cyclin-dependent kinases?
Jorda et al.
J.Med.Chem., 2018;61:9105 -
The cyclin-dependent kinase inhibitors olomoucine and roscovitine arrest human fibroblasts in G1 phase by specific inhibition of CDK2 kinase activity.
Alessi et al.
Exp.Cell.Res., 1998;245:8 -
Cellular effects of olomoucine, an inhibitor of cyclin-dependent kinases.
Abraham et al.
Biol.Cell, 1995;83:105 -
Inhibition of cyclin-dependent kinases by purine analogues.
Vesely et al.
Eur.J.Biochem., 1994;224:771
Product Datasheets
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Citation for Olomoucine
The citations listed below are publications that use Tocris products. Selected citations for Olomoucine include:
1 Citation: Showing 1 - 1
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Association of luteinizing hormone receptor gene expression with cell cycle progression in granulosa cells.
Authors: Cannon Et al.
Am J Physiol Endocrinol Metab 2009;296:E1392
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