2412144-74-0

2412144-74-0 structure
2412144-74-0 structure
  • Name: Aurora A inhibitor 2
  • Chemical Name: Aurora A inhibitor 2
  • CAS Number: 2412144-74-0
  • Molecular Formula: C24H26N6O3
  • Molecular Weight: 446.50
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2022-06-30 19:05:16
  • Modify Date: 2025-08-24 21:42:34
  • Aurora A inhibitor 2 (Compound 16h) is a potent Aurora A kinase inhibitor with an IC50 of 21.94 nM. Aurora A inhibitor 2 induces caspase-dependent apoptosis in MDA-MB-231 cells[1].

Name Aurora A inhibitor 2
Description Aurora A inhibitor 2 (Compound 16h) is a potent Aurora A kinase inhibitor with an IC50 of 21.94 nM. Aurora A inhibitor 2 induces caspase-dependent apoptosis in MDA-MB-231 cells[1].
Related Catalog
Target

Aurora A:21.94 nM (IC50)

Aurora B:273.18 nM (IC50)

In Vitro Aurora A inhibitor 2 (Compound 16h) (0-20 µM, 48 h) shows potent antiproliferative activity against various human cancer cells, and inhibits colony formation[1]. Aurora A inhibitor 2 (0-4 µM, 24 h) inhibits the expression of phosphorylation of Aurora A and Histone H3 in a dose-dependent manner, and induces G2/M cell cycle arrest [1]. Aurora A inhibitor 2 (0-4 µM, 48 h) induces obvious apoptosis in MDA-MB-231 cells in a concentration-dependent manner[1]. Cell Cytotoxicity Assay[1] Cell Line: Breast cancer MDA-MB231, prostate cancer PC3, and neuroblastoma SH-SY5Y cells Concentration: 0-20 µM Incubation Time: 48 h Result: Displayed potent antiproliferative activity with IC50 values of 0.38 ± 0.08, 1.09 ± 0.24, and 0.77 ± 0.12 µM against MDA-MB-231, PC3, and SH-SY5Y cells. Western Blot Analysis[1] Cell Line: MDAMB-231 Concentration: 1, 2, and 4 µM Incubation Time: 24 h Result: A dose-dependent and significant reduction in the phosphorylation of Aurora A and Histone H3 was observed. Significantly increased the levels of cleaved caspase 3/9 and cleaved-PARP. Cell Cycle Analysis[1] Cell Line: MDAMB-231 Concentration: 1, 2, and 4 µM Incubation Time: 24 h Result: Dose-dependently increased the and population of cells in the G2/M phase. Apoptosis Analysis[1] Cell Line: MDAMB-231 Concentration: 1, 2, and 4 µM Incubation Time: 48 h Result: Induced obvious apoptosis in a concentration-dependent manner.
References

[1]. Chengcheng Fan, et al. Design, synthesis, biological evaluation of 6-(2-amino-1H-benzo[d]imidazole-6-yl)quinazolin-4(3H)-one derivatives as novel anticancer agents with Aurora kinase inhibition. Eur J Med Chem. 2020 Mar 15;190:112108.

Molecular Formula C24H26N6O3
Molecular Weight 446.50
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.