您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > STAT3-IN-12
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
STAT3-IN-12
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
STAT3-IN-12图片
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
STAT3-IN-12 是一种有效的STAT3信号抑制剂,可以抑制 IL-6 诱导的 JAK/STAT3 信号通路的激活。STAT3-IN-12 可抑制癌细胞生长、迁移,并诱导细胞凋亡 (apoptosis) 以及周期阻滞。STAT3-IN-12 可用于癌症相关研究,如肝细胞癌 (HCC) 和食管癌。
生物活性

STAT3-IN-12 is a potentSTAT3signal inhibitor that can inhibitIL-6induced JAK/STAT3 signalling pathway activation. STAT3-IN-12 inhibitscancercell growth, migration, and induce cellapoptosisas well as cycle arrest. STAT3-IN-12 can be used in cancer-related research, such as hepatocellular carcinoma (HCC) and oesophageal carcinoma[1].

IC50& Target[1]

STAT3

 

体外研究
(In Vitro)

STAT3-IN-12 (compound 24, 0-10 μM approximately, 72 h) inhibits cancer cell growth and migration in HepG2 and EC109 cells[1].
STAT3-IN-12 (0-20 μM, 16 h) binds to the STAT3 protein and inhibits IL-6-mediated STAT3 phosphorylation, also inhibts STAT3 nuclear localization and dimerization in EC109 and HepG2 cells[1].
STAT3-IN-12 (0-20 μM, 48 h) induces cell apoptosis as well as cycle arrest in HepG2 and EC109 cells[1].

Cell Viability Assay[1]

Cell Line:HepG2 and EC109 cells
Concentration:0, 1.25, 2.5, 5 and 10 μM.
Incubation Time:72 h
Result:Inhibited cancer cell growth with IC50values of 4.32 and 3.63 μM.

Cell Migration Assay[1]

Cell Line:HepG2 and EC109 cells
Concentration:0-10 μM
Incubation Time:24 h
Result:Inhibited cancer cell migration.

Western Blot Analysis[1]

Cell Line:HepG2 and EC109 cells
Concentration:0, 2.5, 5, 10 and 20 μM
Incubation Time:16 h
Result:Inhibited phosphorylation of STAT3 tyrosine 705 with high selectivity.
体内研究
(In Vivo)

STAT3-IN-12 (compound 24, intraperitoneal injection, 20, 40 mg/kg, daily for 24 days) displays obvious antitumor activity in a mouse HepG2 cell xenograft tumor model without no obvious toxicity[1].

Animal Model:HepG2 cell xenograft tumor model[1]
Dosage:20, 40 mg/kg, daily for 24 days
Administration:Intraperitoneal injection
Result:Inhibited tumor growth without affecting the body weight.
分子量

454.56

Formula

C28H30N4O2

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.