Date published: 2026-5-15

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AZ 3146 (CAS 1124329-14-1)

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Alternate Names:
9-cyclopentyl-2-[2-methoxy-4-(1-methylpiperidin-4-yl)oxyanilino]-7-methylpurin-8-one
Application:
AZ 3146 is a potent and selective TTK (monopolar spindle 1 (Mps1) kinase) inhibitor
CAS Number:
1124329-14-1
Purity:
≥98%
Molecular Weight:
452.56
Molecular Formula:
C24H32N6O3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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AZ 3146 is a highly selective inhibitor that targets the mitotic checkpoint kinase Monopolar Spindle 1 (Mps1). By interfering with Mps1, AZ 3146 effectively impedes the proper functioning of the spindle assembly checkpoint (SAC), a regulatory mechanism that ensures accurate chromosome segregation during cell division. This disruption leads to premature anaphase onset, resulting in mitotic errors and, consequently, cell cycle arrest or cell death. Given its unique mechanism of action, AZ 3146 has become useful in cancer research, offering insights into the fundamental processes of mitosis and the potential vulnerabilities of cancer cells that are highly dependent on the SAC for survival. Researchers leverage AZ 3146 to elucidate the role of Mps1 in maintaining genomic stability and to explore new therapeutic strategies targeting the mitotic machinery in various cancer models. Its ability to induce mitotic catastrophe in cancer cells underscores its utility in studying the cellular responses to mitotic errors and the potential for exploiting these errors in the development of anticancer strategies.


AZ 3146 (CAS 1124329-14-1) References

  1. A chemical tool box defines mitotic and interphase roles for Mps1 kinase.  |  Lan, W. and Cleveland, DW. 2010. J Cell Biol. 190: 21-4. PMID: 20624898
  2. Sustained Mps1 activity is required in mitosis to recruit O-Mad2 to the Mad1-C-Mad2 core complex.  |  Hewitt, L., et al. 2010. J Cell Biol. 190: 25-34. PMID: 20624899
  3. Mps1 directs the assembly of Cdc20 inhibitory complexes during interphase and mitosis to control M phase timing and spindle checkpoint signaling.  |  Maciejowski, J., et al. 2010. J Cell Biol. 190: 89-100. PMID: 20624902
  4. Amitozyn impairs chromosome segregation and induces apoptosis via mitotic checkpoint activation.  |  Hermant, B., et al. 2013. PLoS One. 8: e57461. PMID: 23505430
  5. Negative feedback at kinetochores underlies a responsive spindle checkpoint signal.  |  Nijenhuis, W., et al. 2014. Nat Cell Biol. 16: 1257-64. PMID: 25402682
  6. Whole-genome duplication increases tumor cell sensitivity to MPS1 inhibition.  |  Jemaà, M., et al. 2016. Oncotarget. 7: 885-901. PMID: 26637805
  7. Division of labour between PP2A-B56 isoforms at the centromere and kinetochore.  |  Vallardi, G., et al. 2019. Elife. 8: PMID: 30829571
  8. PP1 and PP2A Use Opposite Phospho-dependencies to Control Distinct Processes at the Kinetochore.  |  Smith, RJ., et al. 2019. Cell Rep. 28: 2206-2219.e8. PMID: 31433993
  9. Cyclin B1 scaffolds MAD1 at the kinetochore corona to activate the mitotic checkpoint.  |  Allan, LA., et al. 2020. EMBO J. 39: e103180. PMID: 32202322
  10. Kinetochore phosphatases suppress autonomous Polo-like kinase 1 activity to control the mitotic checkpoint.  |  Cordeiro, MH., et al. 2020. J Cell Biol. 219: PMID: 33125045
  11. Aneuploidy renders cancer cells vulnerable to mitotic checkpoint inhibition.  |  Cohen-Sharir, Y., et al. 2021. Nature. 590: 486-491. PMID: 33505028
  12. Combined morphological and proteome profiling reveals target-independent impairment of cholesterol homeostasis.  |  Schneidewind, T., et al. 2021. Cell Chem Biol. 28: 1780-1794.e5. PMID: 34214450
  13. Chromosomal instability accelerates the evolution of resistance to anti-cancer therapies.  |  Lukow, DA., et al. 2021. Dev Cell. 56: 2427-2439.e4. PMID: 34352222

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

AZ 3146, 10 mg

sc-361114
10 mg
$218.00

AZ 3146, 50 mg

sc-361114A
50 mg
$905.00