Chemical Name: N-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4-piperidinecarboxamide
Biological ActivityCyclin dependent kinase (cdk) inhibitor (reported IC50 values are 0.004 - 0.048, 0.0045 - 0.05, 0.062 - 0.29, 0.2-0.48, 0.4 and 0.45 μM for cdk9, cdk2, cdk7, cdk1, cdk5 and cdk4, respectively). Displays no activity against 190 additional kinases (IC50 >1 μM). Arrests the cell cycle at G2/M; inhibits transcription, proliferation and colony formation, and induces apoptosis in RPMI-8226 multiple myeloma cells. Prevents tumor cell-induced VEGF secretion and in vitro angiogenesis.
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.
How selective are pharmacological inhibitors of cell-cycle-regulating cyclin-dependent kinases?
Jorda et al.
SNS-032 prevents tumor cell-induced angiogenesis by inhibiting vascular endothelial growth factor.
Ali et al.
SNS-032 is a potent and selective CDK 2, 7 and 9 inhibitor that drives target modulation in patient samples.
Conroy et al.
Cancer Chemother.Pharmacol., 2009;64:723
Responses in mantle cell lymphoma cells to SNS-032 depend on the biological context of each cell line.
Chen et al.
Cancer Res., 2010;70:6587
N-(Cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4- piperidinecarboxamide (BMS-387032), a highly efficacious and selective antitumor agent
Misra et al.
Citation for SNS 032
The citations listed below are publications that use Tocris products. Selected citations for SNS 032 include:
1 Citation: Showing 1 - 1
Regulation and function of phosphorylation on VP8, the major tegument protein of bovine herpesvirus 1.
Authors: Zhang Et al.
PLoS One 2015;89:4598
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