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Submit ReviewSNS 032
Description: Cdk inhibitor; potently inhibits cdk2, cdk7 and cdk9
Alternative Names: BMS-387032
Chemical Name: N-[5-[[[5-(1,1-Dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4-piperidinecarboxamide
Purity: ≥99% (HPLC)
Biological Activity for SNS 032
SNS 032 is a cyclin 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.
Technical Data for SNS 032
| M. Wt | 380.53 |
| Formula | C17H24N4O2S2 |
| Storage | Store at -20°C |
| Purity | ≥99% (HPLC) |
| CAS Number | 345627-80-7 |
| PubChem ID | 3025986 |
| InChI Key | OUSFTKFNBAZUKL-UHFFFAOYSA-N |
| Smiles | CC(C)(C)C1=CN=C(CSC2=CN=C(NC(C3CCNCC3)=O)S2)O1 |
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.
Solubility Data for SNS 032
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 19.03 | 50 |
Preparing Stock Solutions for SNS 032
The following data is based on the product molecular weight 380.53. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.5 mM | 5.26 mL | 26.28 mL | 52.56 mL |
| 2.5 mM | 1.05 mL | 5.26 mL | 10.51 mL |
| 5 mM | 0.53 mL | 2.63 mL | 5.26 mL |
| 25 mM | 0.11 mL | 0.53 mL | 1.05 mL |
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Product Datasheets for SNS 032
References for SNS 032
References are publications that support the biological activity of the product.
Misra et al (2004) 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 J.Med.Chem. 47 1719 PMID: 15027863
Ali et al (2007) SNS-032 prevents tumor cell-induced angiogenesis by inhibiting vascular endothelial growth factor. Neoplasia 9 370 PMID: 17534442
Conroy et al (2009) SNS-032 is a potent and selective CDK 2, 7 and 9 inhibitor that drives target modulation in patient samples. Cancer Chemother.Pharmacol. 64 723 PMID: 19169685
Chen et al (2010) Responses in mantle cell lymphoma cells to SNS-032 depend on the biological context of each cell line. Cancer Res. 70 6587 PMID: 20663900
Jorda et al (2018) How selective are pharmacological inhibitors of cell-cycle-regulating cyclin-dependent kinases? J.Med.Chem. 61 9105 PMID: 30234987
If you know of a relevant reference for SNS 032, please let us know.
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Keywords: SNS 032, SNS 032 supplier, SNS032, inhibits, cyclin-depndent, kinase, Cdk, potent, inhibitors, cdk2, cdk7, cdk9, BMS387032, BMS, 387032, BMS-387032, Cyclin-dependent, Kinase, Non-selective, CDKs, 4075, Tocris Bioscience
2 Citations for SNS 032
Citations are publications that use Tocris products. Selected citations for SNS 032 include:
Zhang et al (2015) Regulation and function of phosphorylation on VP8, the major tegument protein of bovine herpesvirus 1. PLoS One 89 4598 PMID: 25673708
Cheung et al (2024) Anti-EGFR antibody-drug conjugate carrying an inhibitor targeting CDK restricts triple-negative breast cancer growth. Clin.Cancer Res. PMID: 38772416
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