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FR 180204

Chemical Structure : FR 180204

CAS No.: 865362-74-9

FR 180204 (FR180204;FR-180204)

Catalog No.: PC-42937Not For Human Use, Lab Use Only.

FR 180204 is a potent, selective, ATP-competitive ERK inhibitor with Ki of 0.31 and 0.14 uM for ERK1 and ERK2, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

FR 180204 is a potent, selective, ATP-competitive ERK inhibitor with Ki of 0.31 and 0.14 uM for ERK1 and ERK2, respectively.
FR 180204 inhibits TGFβ-induced luciferase-expression in mink lung epithelial Mv1Lu cells.
FR 180204 decreases plasma anti-CII antibody levels and attenuates delayed-type hypersensitivity in CII-immunized DBA/1 mice, also inhibits in vitro CII-induced proliferation of lymph node cells prepared from CII-immunized mice.
FR 180204 enhances apoptotic and anti-proliferative effects of Akt inhibitor API-1 in human DLD-1 and LoVo colorectal cancer cells.

Physicochemical Properties

M.Wt 327.3427
Formula C18H13N7
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 50 mg/mL

Chemical Name/SMILES

1H-Pyrazolo[3,4-c]pyridazin-3-amine, 5-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)-

References

1. Ohori M, et al. Biochem Biophys Res Commun. 2005 Oct 14;336(1):357-63.

2. Ohori M, et al. Naunyn Schmiedebergs Arch Pharmacol.

3. Chen-Roetling J, et al. Neuropharmacology. 2009 Apr;56(5):922-8.

4. Saglam AS, et al. Oncol Lett. 2016 Oct;12(4):2463-2474.

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