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  • DC Chemicals Limited
  • China
  • Product Name: STL5-T-0057
  • Price: ¥Inquiry/100mg ¥Inquiry/250mg ¥Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 10 Day
  • Contact: Tony Cao

2756014-24-9

2756014-24-9 structure
2756014-24-9 structure
  • Name: STL5-T-0057
  • Chemical Name: STL5-T-0057
  • CAS Number: 2756014-24-9
  • Molecular Formula: C26H24ClN3O2
  • Molecular Weight: 445.94
  • Catalog: Signaling Pathways Metabolic Enzyme/Protease Aldehyde Dehydrogenase (ALDH)
  • Create Date: 2022-11-21 23:19:42
  • Modify Date: 2024-04-03 18:44:59
  • STL5-T-0057 (compound 68) is an selective ALDH1 B1 inhibitor with an IC50 value of 30 nM. STL5-T-0057 inhibits cell growth of SW480 cells in adherent and spheroid conditions with IC50 values of 2.46 and 0.39 μM, respectively. STL5-T-0057 can be used for the research of cancer[1].

Name STL5-T-0057
Description STL5-T-0057 (compound 68) is an selective ALDH1 B1 inhibitor with an IC50 value of 30 nM. STL5-T-0057 inhibits cell growth of SW480 cells in adherent and spheroid conditions with IC50 values of 2.46 and 0.39 μM, respectively. STL5-T-0057 can be used for the research of cancer[1].
Related Catalog
Target

IC50: 30 nM (ALDH1 B1), 2.46 μM (SW480, adherent), 0.39 μM (SW480, spheroid)[1]

In Vitro STL5-T-0057 (0-10 μM) inhibits ALDH1 B1 with an IC50 value of 30 nM[1]. STL5-T-0057 (0.01-10 μM; 4-5 d) inhibits cell growth of HEK293T cells[1]. STL5-T-0057 (0.01-10 μM) inhibits cell viability of SW480 cells in adherent and spheroid conditions with IC50 values of 2.46 and 0.39 μM, respectively[1]. Cell Cytotoxicity Assay[1] Cell Line: HEK293T cell line Concentration: 0.01-10 μM Incubation Time: 4-5 d Result: Showed cell cytotoxicity to HEK293T cells with a GI50 value of 1.7 μM.
References

[1]. Chen Jame Kenneth, et al. Preparation of substituted imidazolium or cyclic guanidine compounds as isoform-specific aldehyde dehydrogenase inhibitors for the treatment of cancer. WO2021257696 A1. 2021.

Molecular Formula C26H24ClN3O2
Molecular Weight 445.94