FH535
mRNA synthesis
In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
Tyramide Signal Amplification (TSA)
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
Phos Binding Reagent Acrylamide
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
Cell Counting Kit-8 (CCK-8)
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
SYBR Safe DNA Gel Stain
Safe and sensitive stain for visualization of DNA or RNA in agarose or acrylamide gels.
Inhibitor Cocktails
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
FH535 is a small molecule inhibitor of Wnt/B-catenin with IC50 values of 15.4μM, 10.9μM, 9.3μM, respectively in LCSC, Huh7, PLC cell lines [1].
FH535 can inhibit the growth of colon, lung, and hepatocellular carcinoma line but not normal fibroblasts. It makes FH535 potentially be a promising therapeutic approach for cancer cells. It is reported that FH535 has ability to inhibit growth, migration, and invasion of TN breast cancer cell lines (MDA-MB-231 and HCC38) without affecting adhesive abilities of cells to type I collagen [2].
FH535 is also an inhibitor of peroxisome proliferator–activated receptor (PPAR). It plays a role as a dual PPARγ and PPARδ antagonist that is able to inhibit GRIP1 and β-catenin recruitment [3].
References:
[1] Roberto R. Galuppo, Roberto Gedaly, Paul Angulo, Michael F. et al. FH535 inhibits wnt/β-catenin signaling pathway in liver cancer stem cells and HCC cell lines. Hepatology. 2013, October: 466A.
[2] Joji Iida, Jesse Dorchak, John R. Lehman, Rebecca Clancy, Chunqing Luo, Yaqin Chen, Stella Somiari, Rachel E. Ellsworth, Hai Hu, Richard J. Mural, Craig D. Shriver. FH535 Inhibited Migration and Growth of Breast Cancer
Cells. PLOS ONE. 2012, 7(9): 1-11.
[3] Shlomo Handeli and Julian A. Simon. A small-molecule inhibitor of Tcf/β-catenin signaling down-regulates PPARγ and PPARδ activities. Molecular Cancer Therapeutics. 2008, 7:521-529.
| Storage | Store at -20°C |
| M.Wt | 361.2 |
| Cas No. | 108409-83-2 |
| Formula | C13H10Cl2N2O4S |
| Synonyms | FH 535;FH-535 |
| Solubility | ≥36.1 mg/mL in DMSO, ≥5.87 mg/mL in EtOH with gentle warming, <2.26 mg/mL in H2O |
| Chemical Name | 2,5-dichloro-N-(2-methyl-4-nitrophenyl)benzenesulfonamide |
| SDF | Download SDF |
| Canonical SMILES | CC1=C(C=CC(=C1)[N+](=O)[O-])NS(=O)(=O)C2=C(C=CC(=C2)Cl)Cl |
| Shipping Condition | Evaluation sample solution : ship with blue ice.All other available size: ship with RT , or blue ice upon request |
| General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months. |
| Kinase experiment [1]: | |
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High-throughput library screen |
Three copies of the optimized or mutated Tcf-binding element from TOPFLASH or FOPFLASH driving a secreted alkaline phosphatase reporter gene were cloned into pCEP4 plasmid, replacing the cytomegalovirus promoter. The plasmids were transfected into HepG2 cells, and Hygromycin-resistant clones were pooled. Library screening was done at 20 μmol/L concentration in HepG2 serum-free media. Hits were tested in the HCT116 cell line for inhibition of TOPFLASH luciferase activity but not for inhibition of a reporter activity controlled from β-actin promoter. |
| Cell experiment [1]: | |
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Cell lines |
HCT116, SW48, RKO, LoVo, COLO205, IEC6, A427, HCC15, NCI-H1703, A549, HepG2, Hep3b, Huh7 and fibroblasts |
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Preparation method |
The solubility of this compound in DMSO is >10 mM. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
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Reaction Conditions |
30 μM; 48 hrs |
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Applications |
FH535 showed selective anti-proliferation effect on some cancer cells (HCT116, SW48, RKO, LoVo, COLO205, A427, HCC15, NCI-H1703, A549, HepG2, Hep3b and Huh7 cells) expressing high or active Wnt/β-catenin pathway. |
| Animal experiment [2]: | |
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Animal models |
Nude mouse bearing pancreatic cancer xenografts |
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Dosage form |
25 mg/kg; i.p.; every 2 days for 20 days |
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Applications |
FH535 significantly repressed pancreatic cancer xenograft growth in vivo and showed better performance status with respect to body weight loss. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: [1]. Shlomo Handeli and Julian A. Simon. A small-molecule inhibitor of Tcf/β-catenin signaling down-regulates PPARγ and PPARδ activities. Molecular Cancer Therapeutics. 2008, 7:521-529. [2]. Liu L, Zhi Q, Shen M, Gong FR, Zhou BP, Lian L, Shen B, Chen K, Duan W, Wu MY, Tao M, Li W. FH535, a β-catenin pathway inhibitor, represses pancreatic cancer xenograft growth and angiogenesis. Oncotarget. 2016 Jun 13. | |
| Description | FH535 is an inhibitor of Wnt/β-catenin signaling and also an antagonist of dual PPARγ and PPARδ. | |||||
| Targets | PPARγ | PPARδ | Wnt/β-catenin | |||
| IC50 | ||||||
Quality Control & MSDS
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Chemical structure
