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Senexin-A

Chemical Structure : Senexin-A

CAS No.: 1366002-50-7

Senexin-A (Senexin A)

Catalog No.: PC-44628Not For Human Use, Lab Use Only.

Senexin-A is a selective inhibitor of CDK8 (IC50=0.28 uM) and CDK19, inhibits CDK8 and CDK19 ATP site binding with Kd50 of 0.83 uM and 0.31 uM, respectively.

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

Biological Activity

Senexin-A is a selective inhibitor of CDK8 (IC50=0.28 uM) and CDK19, inhibits CDK8 and CDK19 ATP site binding with Kd50 of 0.83 uM and 0.31 uM, respectively.
Senexin-A inhibits only p21-induced transcription but not other biological effects of p21, inhibits β-catenin-dependent transcription in HCT116 colon carcinoma cells.
Senexin-A suppresses damage-induced tumor-promoting paracrine activities of tumor cells and normal fibroblasts.
Senexin-A reverses the increase in tumor engraftment and serum mitogenic activity in mice pretreated with doxorubicin.

Physicochemical Properties

M.Wt 274.32
Formula C17H14N4
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
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Solubility

DMSO: ≥100 mg/mL

Chemical Name/SMILES

6-Quinazolinecarbonitrile, 4-[(2-phenylethyl)amino]-

References

1. Porter DC, et al. Proc Natl Acad Sci U S A. 2012 Aug 21;109(34):13799-804.

2. McDermott MS, et al. Oncotarget. 2017 Feb 21;8(8):12558-12575.

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