A derivative of ARN22089
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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ARN25062

Item No. 39615

Technical Information
Formal Name
6-phenyl-2-(4-piperidinyl)-N-[3-(trifluoromethyl)phenyl]-4-pyrimidinamine
CAS Number
3036492-85-7
Molecular Formula
C22H21F3N4
Formula Weight
Purity
≥95%
A solid
Acetonitrile: Slightly soluble: 0.1-1 mg/mlDMSO: Sparingly soluble: 1-10 mg/ml
SMILES
FC(F)(F)C1=CC=CC(NC2=CC(C3=CC=CC=C3)=NC(C4CCNCC4)=N2)=C1
InChi Code
InChI=1S/C22H21F3N4/c23-22(24,25)17-7-4-8-18(13-17)27-20-14-19(15-5-2-1-3-6-15)28-21(29-20)16-9-11-26-12-10-16/h1-8,13-14,16,26H,9-12H2,(H,27,28,29)
InChi Key
NGGORHPZMJVKNU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ARN25062 is a derivative of ARN22089, an inhibitor of the protein-protein interaction between Cdc42 and p21-activated kinase (PAK).1 It inhibits the proliferation of SKM28, SK-MEL-3, WM3248, and A375 melanoma cells (IC50s = 6.1, 4.6, 9.3, and 5.1 µM, respectively) and SW480 colon cancer cells (IC50 = 5.9 µM). ARN25062 (10 mg/kg) reduces tumor growth in a patient-derived xenograft (PDX) mouse model.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Brindani, N., Vuong, L.M., Acquistapace, I.M., et alDesign, synthesis, in vitro and in vivo characterization of CDC42 GTPase interaction inhibitors for the treatment of cancer. J. Med. Chem. 66(8), 5981-6001 (2023).