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STAT3-IN-13
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-13图片
CAS NO:2248552-86-3
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-13 (compound 6f) 是一种有效的STAT3抑制剂。STAT3-IN-13 具有抗增殖作用,并以 0.46 μM 的KD值与 STAT3 SH2 结构域结合。STAT3-IN-13 抑制 STAT3 Y705 的磷酸化和下游靶基因表达。STAT3-IN-13 在体外诱导细胞凋亡 (apoptosis),在体内抑制肿瘤的生长和转移。STAT3-IN-13 可用于癌症研究。
生物活性

STAT3-IN-13 (compound 6f) is a potentSTAT3inhibitor. STAT3-IN-13 has anti-proliferative effects and binds to theSTAT3SH2 domain with a KDof 0.46 μM. STAT3-IN-13 inhibits the phosphorylation ofSTAT3Y705 and downstream target gene expression. STAT3-IN-13 inducesapoptosisin vitro and suppresses the growth and metastasis of tumor in vivo. STAT3-IN-13 can be used forcancerresearch[1].

体外研究
(In Vitro)

STAT3-IN-13 (compound 6f) (48 hours) has anti-proliferative activity with IC50values of 0.25, 0.11 and 0.55 μM for 143B, HOS and MG63 cells, respectively[1].
STAT3-IN-13 (compound 6f) (0.001-100 μM) binds to STAT3 and interacts with STAT3586–685in a concentration dependent manner with a KDof 0.96 μM[1].
STAT3-IN-13 (compound 6f) (0-1.0 μM; 24 hours; 143B and HOS cells) inhibits STAT3 Y705 phosphorylation and suppresses STAT3 in tumor cells[1].
STAT3-IN-13 (compound 6f) (0-1.0 μM; 48 hours; 143B cells) induces apoptosis in a dose-dependent manner[1].

Apoptosis Analysis[1]

Cell Line:143B cells
Concentration:0, 0.2, 0.5, and 1 μM
Incubation Time:48 hours
Result:Increased the percentage of apoptosis rates of 3.4%, 8.7%, 10.7%, and 23.3% at 0, 0.2, 0.5 and 1 μM, respectively.

Western Blot Analysis[1]

Cell Line:143B and HOS cells
Concentration:0, 0.2, 0.5 and 1.0 μM
Incubation Time:24 hours
Result:Inhibited STAT3 Y705 phosphorylation and downstream target gene expression including Bcl-2 and VEGF, retained good antitumor activities against control tumor cells without STAT3 knockdown.
体内研究
(In Vivo)

STAT3-IN-13 (compound 6f) (10-20 mg/kg; i.p.; twice daily, for 4 weeks; nude mice) blocks osteosarcoma growth and metastasis in vivo[1].

Animal Model:Nude mice
Dosage:10 and 20 mg/kg
Administration:Intraperitoneal injection; twice daily, for 4 weeks
Result:Suppressed tumor weight at a dose of 10 mg/kg.
分子量

436.49

Formula

C21H20N6O3S

CAS 号

2248552-86-3

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.