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  • DC Chemicals Limited
  • China
  • Product Name: THZ-P1-2
  • Price: $Inquiry/250mg $Inquiry/100mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

2058075-45-7

2058075-45-7 structure
2058075-45-7 structure
  • Name: THZ-P1-2
  • Chemical Name: THZ-P1-2
  • CAS Number: 2058075-45-7
  • Molecular Formula: C31H29N7O2
  • Molecular Weight: 531.61
  • Catalog: Signaling Pathways Autophagy Autophagy
  • Create Date: 2020-06-01 16:43:20
  • Modify Date: 2024-01-10 10:58:48
  • THZ-P1-2 is a potent and selective PI5P4K inhibitor. THZ-P1-2 covalently targets cysteines on a disordered loop in PI5P4Kα/β/γ with an IC50 of 190 nM for PI5P4Kα. THZ-P1-2 causes autophagy disruption and upregulates TFEB signaling. THZ-P1-2 displays anticancer activity in leukemia cell lines[1].

Name THZ-P1-2
Description THZ-P1-2 is a potent and selective PI5P4K inhibitor. THZ-P1-2 covalently targets cysteines on a disordered loop in PI5P4Kα/β/γ with an IC50 of 190 nM for PI5P4Kα. THZ-P1-2 causes autophagy disruption and upregulates TFEB signaling. THZ-P1-2 displays anticancer activity in leukemia cell lines[1].
Related Catalog
In Vitro THZ-P1-2 (0.2-11.4 μM) exhibits approximately 75% inhibition of PI-4,5-P2 formation by PI5P4Kα and PI5P4Kγ and 50% inhibition by PI5P4Kβ at a concentration of 0.7 μM[1]. THZ-P1-2 (10-100000 nM; 72 hours) shows modest anti-proliferative activity in all six AML/ALL cell lines with IC50 values in the low micromolar range[1]. Cell Proliferation Assay[1] Cell Line: THP1, SEMK2, OCI/AML-2, HL60, SKM1, NOMO1 cells Concentration: 10-100000 nM Incubation Time: 72 hours Result: Showed anti-proliferative activity in all six AML/ALL cell lines with IC50 values ranging from 0.87 to 3.95 μM.
References

[1]. Sivakumaren SC, et al. Targeting the PI5P4K Lipid Kinase Family in Cancer Using Covalent Inhibitors. Cell Chem Biol. 2020;27(5):525‐537.e6.

Molecular Formula C31H29N7O2
Molecular Weight 531.61