Tubulin polymerization-IN-11

Modify Date: 2025-08-26 10:30:41

Tubulin polymerization-IN-11 Structure
Tubulin polymerization-IN-11 structure
Common Name Tubulin polymerization-IN-11
CAS Number 2470063-59-1 Molecular Weight 406.43
Density N/A Boiling Point N/A
Molecular Formula C22H22N4O4 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Tubulin polymerization-IN-11


Tubulin polymerization-IN-11 is a potent tubulin polymerization inhibitor with an IC50 value of 3.4 µM. Tubulin polymerization-IN-11 shows antiproliferative activity. Tubulin polymerization-IN-11 induces Apoptosis and cell cycle arrest at G2/M phase. Tubulin polymerization-IN-11 decreases the expression of cyclin B1, p-cdc2, and Bcl-2 protein levels and increases the expression of cleaved PARP[1].

 Names

Name Tubulin polymerization-IN-11

 Tubulin polymerization-IN-11 Biological Activity

Description Tubulin polymerization-IN-11 is a potent tubulin polymerization inhibitor with an IC50 value of 3.4 µM. Tubulin polymerization-IN-11 shows antiproliferative activity. Tubulin polymerization-IN-11 induces Apoptosis and cell cycle arrest at G2/M phase. Tubulin polymerization-IN-11 decreases the expression of cyclin B1, p-cdc2, and Bcl-2 protein levels and increases the expression of cleaved PARP[1].
Related Catalog
In Vitro Tubulin polymerization-IN-11 (compound 7i) (0-100 µM; 48 h) 显示抗增殖活性,对HeLa, HEK-293, A549, MCF-7, T47D 细胞的 IC50 值分别为 0.012、>100 µM、10.40、40.40、27.91 µM[1]. Tubulin polymerization-IN-11 (12, 24, 48 nM; 24 h) 以剂量依赖的方式诱导细胞凋亡和细胞周期停滞在 G2/M 期[1]。 Tubulin polymerization-IN-11 (12, 24, 48 nM; 24 h) 以剂量依赖性方式降低细胞周期蛋白 B1、p-cdc2、Bcl-2 蛋白水平并增加 cleaved PARP 蛋白的表达[ 1]。 Cell Proliferation Assay[1] Cell Line: HeLa, HEK-293, A549, MCF-7, T47D cells Concentration: 0-100 µM Incubation Time: 48 h Result: Showed antiproliferative activity with IC50s of 0.012, >100, 10.40, 40.40, 27.91 µM for HeLa, HEK-293, A549, MCF-7, T47D cells, respectively. Cell Cycle Analysis[1] Cell Line: HeLa cells Concentration: 12, 24, 48 nM Incubation Time: 24 h Result: Induced cell cycle arrest at G2/M phase with the percentage of cells was 13.90%, 26.00%, and 92.65% at 12, 24, 48 nM, respectively. Western Blot Analysis[1] Cell Line: HeLa cells Concentration: 12, 24, 48 nM Incubation Time: 24 h Result: Concentration-dependently decreased cyclin B1 and p-cdc2 protein levels. Apoptosis Analysis[1] Cell Line: HeLa cells Concentration: 12, 24, 48 nM Incubation Time: 24 h Result: Induced apoptosis with the total numbers of early and late apoptotic cells were 8.44%, 26.87% and 53.3% at 12, 24, and 48 nM, respectively.
References

[1]. Yang F, et al. Synthesis, and biological evaluation of 3,6-diaryl-[1,2,4]triazolo[4,3-a]pyridine analogues as new potent tubulin polymerization inhibitors. Eur J Med Chem. 2020 Oct 15;204:112625.

 Chemical & Physical Properties

Molecular Formula C22H22N4O4
Molecular Weight 406.43
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.