Top Suppliers:I want be here

2675490-72-7

2675490-72-7 structure
2675490-72-7 structure
  • Name: DIZ-3
  • Chemical Name: DIZ-3
  • CAS Number: 2675490-72-7
  • Molecular Formula: C46H44F2N8
  • Molecular Weight: 746.89
  • Catalog: Signaling Pathways Cell Cycle/DNA Damage G-quadruplex
  • Create Date: 2023-05-31 07:43:01
  • Modify Date: 2024-02-03 10:53:56
  • DIZ-3 is a selective multimeric G4 ligand based on a G4-ligand-dimerizing strategy. DIZ-3 intercalates into the G4-G4 interface, stabilizing the higher-order structure. DIZ-3 induces cell cycle arrest and apoptosis, and thus inhibits cell proliferation in alternative lengthening of telomere (ALT) cancer cells[1].

Name DIZ-3
Description DIZ-3 is a selective multimeric G4 ligand based on a G4-ligand-dimerizing strategy. DIZ-3 intercalates into the G4-G4 interface, stabilizing the higher-order structure. DIZ-3 induces cell cycle arrest and apoptosis, and thus inhibits cell proliferation in alternative lengthening of telomere (ALT) cancer cells[1].
Related Catalog
In Vitro DIZ-3 (0-40 μM; 24 小时) 抑制 ALT 癌细胞系的增殖[1]。 DIZ-3 (0.6-2.5 μM; 24小时) 诱导 U2OS 细胞周期停滞和细胞凋亡[1]。 DIZ-3 (0.12, 0.25, 0.5 μM; 7 天) 导致 U2OS 细胞集落形成[1]。 DIZ-3 (0.12, 0.25, 0.5 μM; 24小时) 显着抑制 U2OS 细胞的迁移[1]。 Cell Proliferation Assay[1] Cell Line: Human bone osteosarcoma U2OS cells, normal BJ fibroblasts Concentration: 0-40 μM Incubation Time: 24 hours Result: Caused a significant dose-dependent cytotoxic effect on U2OS cancer cells with an IC50 of 2.1 µM. Induced much weaker growth inhibition on normal BJ fibroblasts with an IC50 of 29.3 µM. Apoptosis Analysis[1] Cell Line: U2OS cells Concentration: 0.6, 1.2, 2.5 μM Incubation Time: 24 hours Result: Induced significant apoptosis in U2OS cells (the percentage of apoptotic cells increased from 10.1% to 24.9%). Cell Cycle Analysis[1] Cell Line: U2OS cells Concentration: 0.6, 1.2, 2.5 μM Incubation Time: 24 hours Result: Induced the apparent accumulation of cells in the S phase (increasing from 24.0% to 32.2%) in a dose-dependent manner.
References

[1]. Ming-Hao Hu, et al. Dimeric aryl-substituted imidazoles may inhibit ALT cancer by targeting the multimeric G-quadruplex in telomere. Eur J Med Chem. 2020 Jan 15;186:111891.  

Molecular Formula C46H44F2N8
Molecular Weight 746.89
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.