Chemical Structure : CIP2A inhibitor TD52
CAS No.: 1798328-24-1
货号: PC-23570Not For Human Use, Lab Use Only.
TD52 is a small molecule inhibitor of cancerous inhibitor of protein phosphatase 2A (CIP2A), downregulates CIP2A and p-Akt, reactivates protein phosphatase 2A.
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---|---|---|---|
5 mg | ¥780 | In stock | |
10 mg | ¥1180 | In stock | |
25 mg | ¥2180 | In stock | |
50 mg | ¥3580 | In stock | |
100 mg | Get quote |
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TD52 is a small molecule inhibitor of cancerous inhibitor of protein phosphatase 2A (CIP2A), downregulates CIP2A and p-Akt, reactivates protein phosphatase 2A.
TD52 causes greater reduction in cell viability than erlotinib in all the HCC cell lines tested including HA22T (IC50=0.9 μmol/l), Hep3B (IC50=0.9 μmol/l), PLC5 (IC50=0.8 μmol/l) and Sk-Hep1 (IC50=1.2 μmol/l), which is independent of EGFR kinase inhibition.
TD52 downregulates the protein expression of CIP2A and p-Akt in a dose- and time-dependent manner, with no effect on the expression level of PP2A-related subunits, PP2A-A, PP2A-B55 and PP2A-C.
TD52 downregulates transcription of CIP2A via interfering Elk-1 function.
TD52 (10 mg/kg/day) exhibits in vivo antitumor effects on a PLC5 xenograft tumor model.
分子量 | 360.42 | |
分子式 | C24H16N4 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
N2,N3-Bis(3-ethynylphenyl)quinoxaline-2,3-diamine |
1. Yu HC, et al. Cell Death Dis. 2014 Jul 31;5(7):e1359.
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