STAT3-IN-1 |
| カタログ番号GC37688 |
STAT3-IN-1 (化合物 7d) は、HT29 細胞および MDA-MB 231 細胞でそれぞれ 1.82 μM および 2.14 μM の IC50 値を持つ、優れた選択的かつ経口的に活性な STAT3 阻害剤です。 STAT3-IN-1 (化合物 7d) は腫瘍のアポトーシスを誘導します。
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 2059952-75-7
Sample solution is provided at 25 µL, 10mM.
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STAT3-IN-1 (compound 7d) is an excellent, selective and orally active STAT3 inhibitor, with IC50 values of 1.82 μM and 2.14 μM in HT29 and MDA-MB 231 cells, respectively. STAT3-IN-1 (compound 7d) induces tumor apoptosis[1]. IC50: 1.82 μM (STAT3 in HT29 cells), 2.14 μM (STAT3 in MDA-MB 231 cells)[1].
STAT3-IN-1 (compound 7d: 0-10 μM, 48 h) inhibits the STAT3 acetylation at lysine 685 and affected its specific genes expressions[1].STAT3-IN-1 (compound 7d: 0-10 μM, 48 h) induces tumor cells apoptosis in MDA-MB-231 cells[1]. Apoptosis Analysis[1] Cell Line: MDA-MB-231 cell lines.
STAT3-IN-1 (compound 7d: 10, 20 mg/kg, two weeks) arrests tumor growth with low toxicity in mouse-xenograft model[1]. Animal Model: Mouse-xenograft model bearing inoculation of mice breast cancer 4T1 cells[1].
[1]. Li S, et al. Discovery of oral-available resveratrol-caffeic acid based hybrids inhibiting acetylated and phosphorylated STAT3 protein. Eur J Med Chem. 2016 Nov 29;124:1006-1018.
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