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2361304-26-7

中文名稱 STAT3-IN-3
英文名稱 STAT3-IN-3
CAS 2361304-26-7
分子式 C27H26BrN3O6S
分子量 600.48
MOL 文件 2361304-26-7.mol
2361304-26-7 結(jié)構(gòu)式 2361304-26-7 結(jié)構(gòu)式

基本信息

中文別名
化合物 T13010
英文別名
STAT3-IN-3
STAT3 inhibitor 3
2H-1-Benzopyran-2-one, 3-[[4-[(4-bromo-1,1-dioxidobenzo[b]thien-2-yl)carbonyl]-1-piperazinyl]carbonyl]-7-(diethylamino)-

物理化學(xué)性質(zhì)

沸點915.1±65.0 °C(Predicted)
密度1.572±0.06 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度DMSO: 5 mg/mL (8.33 mM)
酸度系數(shù)(pKa)3.19±0.20(Predicted)
形態(tài)Solid
顏色Light yellow to yellow

常見問題列表

生物活性
STAT3-IN-3 是一種有效和選擇性的 STAT3 抑制劑,有抗增殖活性。STAT3-IN-3 可以引起乳腺癌細(xì)胞凋亡 (apoptosis)。STAT3-IN-3 是有前途的靶向線粒體的 STAT3 抑制劑,能用于癌癥的研究。
靶點

STAT3

體外研究

STAT3-IN-3 has no influence on the phosphorylation levels of STAT1, JAK2, Src and Erk1/2.
STAT3-IN-3 inhibits the growth of MDA-MB-231, HCT-116, HepG2, and MCF-7 cells with IC 50 s of 1.43 μM, 1.89 μM, 2.88 μM, and 3.33 μM, respectively.
STAT3-IN-3 down-regulates the expression of STAT3 target genes Bcl-2 and Cyclin D1.
STAT3-IN-3 inhibits STAT3 tyrosine phosphorylation and serine phosphorylation.
STAT3-IN-3 inhibits STAT3 DNA-binding activity.
STAT3-IN-3 (1-4 μM; 24 hours) increases ROS production and remarkably reduces the mitochondrial membrane potential to induce mitochondrial apoptotic pathway.
STAT3-IN-3 (1-4 μM; 24 hours) can induce the cleavage of caspase-9, caspase-3 and PARP.

Cell Viability Assay

Cell Line: MDA-MB-231 cells, HCT-116 cells, HepG2 cells, MCF-7cells
Concentration: MTT assay
Incubation Time: 48 hours
Result: Exhibited anti-proliferative activity.

Apoptosis Analysis

Cell Line: MDA-MB-231 cells
Concentration: 0 μM, 1 μM, 2 μM, 4 μM
Incubation Time: 24 hours
Result: Induced the apoptosis of MDA-MB-231 cells dose-dependently and the apoptosis rates.

Western Blot Analysis

Cell Line: MDA-MB-231 cells
Concentration: 0 μM, 1 μM, 2 μM, 4 μM
Incubation Time: 24 hours
Result: Induced the cleavage of caspase-9, caspase-3 and PARP.
體內(nèi)研究

STAT3-IN-3 (10mg/kg-20 mg/kg; i.p.; daily; for 14 days) possesses potent antitumor activity against implanted 4T1 breast tumors growth.

Animal Model: Adult female BALB/c mice (6 weeks of age)
Dosage: 10 mg/kg, 20 mg/kg
Administration: Intraperitoneal injection, daily, for 14 days
Result: Significantly inhibited tumor volume.
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