Date published: 2026-4-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Cdk1/2 Inhibitor III (CAS 443798-55-8)

5.0(1)
Write a reviewAsk a question

See product citations (3)

Alternate Names:
5-Amino-3-((4-(aminosulfonyl)phenyl)amino)-N-(2,6-difluorophenyl)-1H-1,2,4-triazole-1-carbothioamide
Application:
Cdk1/2 Inhibitor III is A cell-permeable triazolo-diamine compound and ATP inhibitor
CAS Number:
443798-55-8
Purity:
>95%
Molecular Weight:
425.44
Molecular Formula:
C15H13F2N7O2S2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Cdk1/2 Inhibitor III is a synthetic molecule specifically designed to target and inhibit the activity of cyclin-dependent kinases 1 and 2 (Cdk1 and Cdk2), which are essential enzymes in the regulation of the cell cycle. These kinases play critical roles in controlling the progression of cells through various phases of the cell cycle, particularly the G1/S and the G2/M transitions. Cdk1/2 Inhibitor III works by interfering with the ATP-binding site of these enzymes, thereby preventing their catalytic activity and halting cell cycle progression. The inhibition of Cdk1 and Cdk2 disrupts the phosphorylation of key proteins required for cell cycle progression, leading to cell cycle arrest. This mechanism is especially relevant in the study of cellular proliferation and oncogenesis, where uncontrolled cell division is a hallmark. By selectively targeting these kinases, Cdk1/2 Inhibitor III serves as a powerful tool in cell biology and cancer research, allowing scientists to dissect the complex signaling networks that govern cell cycle regulation.


Cdk1/2 Inhibitor III (CAS 443798-55-8) References

  1. Varicella-zoster virus IE63 protein phosphorylation by roscovitine-sensitive cyclin-dependent kinases modulates its cellular localization and activity.  |  Habran, L., et al. 2005. J Biol Chem. 280: 29135-43. PMID: 15955820
  2. 1-Acyl-1H-[1,2,4]triazole-3,5-diamine analogues as novel and potent anticancer cyclin-dependent kinase inhibitors: synthesis and evaluation of biological activities.  |  Lin, R., et al. 2005. J Med Chem. 48: 4208-11. PMID: 15974571
  3. Induction of asymmetrical cell division to analyze spindle-dependent organelle partitioning using correlative microscopy techniques.  |  Wei, JH. and Seemann, J. 2009. Nat Protoc. 4: 1653-62. PMID: 19876022
  4. Cyclin-dependent kinase 5 phosphorylates endothelial nitric oxide synthase at serine 116.  |  Cho, DH., et al. 2010. Hypertension. 55: 345-52. PMID: 20048197
  5. Taiwan cobra cardiotoxin III inhibits Src kinase leading to apoptosis and cell cycle arrest of oral squamous cell carcinoma Ca9-22 cells.  |  Chien, CM., et al. 2010. Toxicon. 56: 508-20. PMID: 20493203
  6. Kinase inhibitor profile for human nek1, nek6, and nek7 and analysis of the structural basis for inhibitor specificity.  |  Moraes, EC., et al. 2015. Molecules. 20: 1176-91. PMID: 25591119
  7. Polydatin inhibits the oxidative stress-induced proliferation of vascular smooth muscle cells by activating the eNOS/SIRT1 pathway.  |  Ma, Y., et al. 2016. Int J Mol Med. 37: 1652-60. PMID: 27081912
  8. Methods and sensors for functional genomic studies of cell-cycle transitions in single cells.  |  Zambon, AC., et al. 2020. Physiol Genomics. 52: 468-477. PMID: 32866086
  9. Altered G1 signaling order and commitment point in cells proliferating without CDK4/6 activity.  |  Liu, C., et al. 2020. Nat Commun. 11: 5305. PMID: 33082317
  10. Nuclear-cytoplasmic compartmentalization of cyclin B1-Cdk1 promotes robust timing of mitotic events.  |  Maryu, G. and Yang, Q. 2022. Cell Rep. 41: 111870. PMID: 36577372

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Cdk1/2 Inhibitor III, 1 mg

sc-202530
1 mg
$198.00