A JNK3 inhibitor
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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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SR 3576

Item No. 20215

Technical Information
Formal Name
3-[4-[[[(3-methylphenyl)amino]carbonyl]amino]-1H-pyrazol-1-yl]-N-(3,4,5-trimethoxyphenyl)-benzamide
CAS Number
1164153-22-3
Molecular Formula
C27H27N5O5
Formula Weight
Purity
≥98%
A solid
DMSO: 40 mg/ml
SMILES
CC1=CC=CC(NC(NC2=CN(C3=CC=CC(C(NC4=CC(OC)=C(OC)C(OC)=C4)=O)=C3)N=C2)=O)=C1
InChi Code
InChI=1S/C27H27N5O5/c1-17-7-5-9-19(11-17)30-27(34)31-21-15-28-32(16-21)22-10-6-8-18(12-22)26(33)29-20-13-23(35-2)25(37-4)24(14-20)36-3/h5-16H,1-4H3,(H,29,33)(H2,30,31,34)
InChi Key
MTFAYLZZDJGFGV-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    SR 3576 is a JNK3 inhibitor (IC50 = 7 nM).1 It is selective for JNK3 over JNK1 and p38 MAP kinase (IC50s = 0.17 and >20 µM, respectively). It inhibits c-Jun phosphorylation in INS-1 cells (IC50 = 1.3 µM).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kamenecka, T., Habel, J., Duckett, D., et alStructure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38. The Journal of Biological Chemisty 284(19), 12853-12861 (2009).