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AS601245

Cat. No. M10633

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AS601245 Structure
Synonym:

AS-601245

Size Price Availability Quantity
1mg USD 48 In stock
5mg USD 120 In stock
10mg USD 200 In stock
50mg USD 780 In stock
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Quality Control & Documentation
Biological Activity

AS601245 is an orally active, selective, ATP competitive JNK (c-Jun NH2-terminal protein kinase) inhibitor with IC50 values of 150, 220, and 70 nM for JNK human isoforms (hJNK1, hJNK2, and hJNK3), respectively. AS601245 and Clofibrate have a synergistic effect in inducing cell responses and in affecting the gene expression profile in CaCo-2 colon cancer cells.

In vivo, AS601245 (40, 60, and 80 mg/kg; i.p.) provides significant protection against the delayed loss of hippocampal CA1 neurons in a gerbil model of transient global ischemia. AS601245 (0.3-10 mg/kg; p.o.) is a potent inhibitor of LPS-induced TNF-α release in mice.

Chemical Information
Molecular Weight 372.45
Formula C20H16N6S
CAS Number 345987-15-7
Solubility (25°C) DMSO 6 mg/mL (May need ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Qinghua Wu, et al. J Enzyme Inhib Med Chem . Selective inhibitors for JNK signalling: a potential targeted therapy in cancer

[2] Angelo Cerbone, et al. PLoS One . Rosiglitazone and AS601245 decrease cell adhesion and migration through modulation of specific gene expression in human colon cancer cells

[3] Sonia Carboni, et al. J Pharmacol Exp Ther . AS601245 (1,3-benzothiazol-2-yl (2-[[2-(3-pyridinyl) ethyl] amino]-4 pyrimidinyl) acetonitrile): a c-Jun NH2-terminal protein kinase inhibitor with neuroprotective properties

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Keywords: AS601245, AS-601245 supplier, JNK, inhibitors, activators

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