tcsc1538 FH535

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Product Description

FH535 is an inhibitor of Wnt/β-catenin and PPAR, with anti-tumor activities.

IC50 & Target: Wnt, β-catenin, PPAR[1]

In Vitro: FH535 is an inhibitor of Wnt/β-catenin and PPAR. FH535 inhibits PPARγ and PPARδ transactivation in HCT116 cells. FH535 (15 μM) activities depend on functional PPARδ but does not require a cysteine residue in the PPAR ligand-binding domain. FH535 inhibits recruitment of the coactivators GRIP1 and β-catenin to PPARδ and PPARγ. FH535 shows toxic effects on 12 carcinoma cell lines expressing wnt/β-catenin pathway[1]. FH535 (20 μM) suppresses the β-catenin pathway in pancreatic cancer cells, and inhibits pancreatic cancer cell migration. Furthermore, FH535 (20, 40 μM) inhibits pancreatic cancer cell invasion and cell growth[2]. FH535 represses angiogenesis-related genes in pancreatic cancer cells[3].

In Vivo: FH535 (25 mg/kg, i.p.) exhibits an anti-tumor effect on pancreatic cancer xenografts in mice. FH535 also represses angiogenesis in pancreatic cancer xenografts[2].

Information

CAS No108409-83-2
FormulaC13H10Cl2N2O4S
Clinical Informationclinicalinformation
PathwayCell Cycle/DNA Damage
Stem Cell/Wnt
Stem Cell/Wnt
TargetPPAR
β-catenin
Wnt

Specifications

Purity / Grade>98%
SolubilityDMSO : 33.33 mg/mL (92.28 mM; Need ultrasonic); H2O : < 0.1 mg/mL (insoluble)
Smilessmiles

Misc Information

Observed Molecular Weight361.2
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