首页-
Products -
Apoptosis -
Apoptosis -
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
CAS No. 1313019-65-6
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea ( SC-1 )
产品货号. M27576 CAS No. 1313019-65-6
SC-1 是多种酪氨酸激酶抑制剂索拉非尼的衍生物。 SC-1 通过阻断 STAT3 磷酸化和激活来有效抑制 STAT3 磷酸化,并诱导肝细胞癌细胞系凋亡。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥2203 | 有现货 |
|
| 10MG | ¥3467 | 有现货 |
|
| 25MG | ¥6302 | 有现货 |
|
| 50MG | ¥9072 | 有现货 |
|
| 100MG | ¥12069 | 有现货 |
|
| 200MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述SC-1 是多种酪氨酸激酶抑制剂索拉非尼的衍生物。 SC-1 通过阻断 STAT3 磷酸化和激活来有效抑制 STAT3 磷酸化,并诱导肝细胞癌细胞系凋亡。
-
产品描述SC-1 is a a derivative of the multiple tyrosine kinase inhibitor sorafenib. SC-1 potently inhibits the phosphorylation of STAT3 by blocking STAT3 phosphorylation and activation, and induces apoptosis in hepatocellular carcinoma cell lines.(In Vitro):SC-1(1-10 μM; 48 hours; breast cancer cells) treatment demonstrates dose-dependent suppression of cell viability in all tested breast cancer cells. SC-1(1-10 μM; 36 hours; breast cancer cells) treatment induces potent apoptotic activity in association with downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines.(In Vivo):SC-1 showes efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors in vivo.
-
体外实验STAT3-IN-7 (SC-1; 1-10 μM; 48 hours; breast cancer cells) treatment demonstrates dose-dependent suppression of cell viability in all tested breast cancer cells.STAT3-IN-7 (SC-1; 1-10 μM; 36 hours; breast cancer cells) treatment induces potent apoptotic activity.STAT3-IN-7 (SC-1; 1-10 μM; 36 hours; breast cancer cells) treatment shows downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines. Cell Viability AssayCell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:48 hours Result:Demonstrated dose-dependent suppression of cell viability in all tested breast cancer cells.Apoptosis Analysis Cell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:36 hours Result:Induced potent apoptotic activity.Western Blot Analysis Cell Line:HCC-1937, MDA-MB-231, MDA-MB-468, MDA-MB-453, SK-BR3 and MCF-7 cells Concentration:1 μM, 2 μM, 5 μM, 7.5 μM, 10 μM Incubation Time:36 hoursResult:Showed downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines.
-
体内实验STAT3-IN-7 (10 mg/kg; oral gavage; daily; for 28 days; female NCr athymic nude mice) treatment shows efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors. Animal Model:Female NCr athymic nude mice (4-6 weeks of age) injected with breast cancer cells Dosage:10 mg/kg Administration:Oral gavage; daily; for 28 days Result:Showed efficacious antitumor activity and p-STAT3 downregulation in MDA-MB-468 xenograft tumors.
-
同义词SC-1
-
通路Apoptosis
-
靶点Apoptosis
-
受体HCV|Bacterial|Apoptosis|Fungal
-
研究领域——
-
适应症——
化学信息
-
CAS Number1313019-65-6
-
分子量431.8
-
分子式C21H13ClF3N3O2
-
纯度>98% (HPLC)
-
溶解度In Vitro:?DMSO : 250 mg/mL (578.97 mM)
-
SMILESN#Cc(cc1)ccc1Oc(cc1)ccc1NC(Nc(cc1)cc(C(F)(F)F)c1Cl)=O
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Satoru Tamura, et al. Oenothein B, dimeric hydrolysable tannin inhibiting HCV invasion from Oenothera erythrosepala. J Nat Med. 2019 Jan;73(1):67-75.
产品手册
关联产品
-
(±)-Indoxacarb
Indoxacarb ((±)-Indoxacarb; DPX-JW062) 是一种广谱恶二嗪类杀虫剂,具有高杀虫活性和低哺乳动物毒性。Indoxacarb 阻断神经制剂和分离神经元中的昆虫钠通道 (sodium channels) (Sodium Channel)。
-
CMLD-2
CMLD-2 是一种 HuR-ARE 相互作用 的抑制剂。CMLD-2 竞争性结合 HuR 蛋白,破坏其与富含腺嘌呤-尿苷元素 (ARE) 的 mRNA 靶标的相互作用 (Ki=350 nM)。CMLD-2 可诱导凋亡并在结肠癌,胰腺癌,甲状腺癌和肺癌细胞系中表现出抗肿瘤活性。Hu 抗原 R (HuR) 是一种 RNA 结合蛋白,可以调节靶标 mRNA 的稳定性和翻译。
-
Neoisoliquiritin b
Neoisoliquiritigenin, isolated from Spatholobus suberectus, inhibits cell proliferation and induces cell apoptosis in breast cancer by directly binding to GRP78 to regulate the β-catenin pathway
021-51111890
购物车()
sales@molnova.cn

