2432825-93-7

2432825-93-7 structure
2432825-93-7 structure
  • Name: HDAC8-IN-3
  • Chemical Name: HDAC8-IN-3
  • CAS Number: 2432825-93-7
  • Molecular Formula: C18H12N4O3S2
  • Molecular Weight: 396.44
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2022-08-17 13:04:42
  • Modify Date: 2025-08-21 12:20:57
  • HDAC8-IN-3 (compound P19) is a potent HDAC8 inhibitor with IC50 value of 9.3 μM and produces thermal stabilization. HDAC8-IN-3 has cytotoxicity and induces apoptosis in leukemic cell lines[1].

Name HDAC8-IN-3
Description HDAC8-IN-3 (compound P19) is a potent HDAC8 inhibitor with IC50 value of 9.3 μM and produces thermal stabilization. HDAC8-IN-3 has cytotoxicity and induces apoptosis in leukemic cell lines[1].
Related Catalog
Target

HDAC8:9.3 μM (IC50)

HDAC4:>50 μM (IC50)

HDAC1:>50 μM (IC50)

HDAC2:41 μM (IC50)

HDAC3:>50 μM (IC50)

HDAC5:>50 μM (IC50)

HDAC6:17 μM (IC50)

HDAC8:>50 μM (IC50)

In Vitro HDAC8-IN-3 (compound P19) (5-200 μM, 48 hours; HEK293T cells) has cytotoxicity in leukemic cell lines[1]. HDAC8-IN-3 (compound P19) (50 μM) inhibits glucose transporter 1 (GLUT1)-mediated glucose transport by down-regulating GLUT1 expression (IC50 = 28.2 μM)[1]. HDAC8-IN-3 (compound P19) (79.9 μM; 24 hours) can induce apoptotic death in the CEM cell line[1]. Cell Cytotoxicity Assay[1] Cell Line: K562, KCL22 and CEM leukemia cells. Concentration: 50 μM Incubation Time: 48 hours Result: Inhibited with IC50 values of 79.9, 85.4 and 43.2 μM for CEM, K562 and KCL22 cells, respectively. Apoptosis Analysis[1] Cell Line: CEM cells Concentration: 79.9 μM Incubation Time: 24 hours Result: The percentage of apoptotic cells was recorded as 60.97%.
References

[1]. Upadhyay N, et al. Discovery of novel N-substituted thiazolidinediones (TZDs) as HDAC8 inhibitors: in-silico studies, synthesis, and biological evaluation. Bioorg Chem. 2020 Jul;100:103934.

Molecular Formula C18H12N4O3S2
Molecular Weight 396.44
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