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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 | ¥708 | 有现货 |
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| 10MG | ¥1131 | 有现货 |
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| 25MG | ¥2353 | 有现货 |
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| 50MG | ¥3692 | 有现货 |
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| 100MG | ¥5265 | 有现货 |
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| 200MG | ¥7101 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥839 | 有现货 |
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生物学信息
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产品名称1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea
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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
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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。
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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.
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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.
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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.
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同义词SC-1
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通路Apoptosis
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靶点Apoptosis
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受体HCV|Bacterial|Apoptosis|Fungal
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研究领域——
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适应症——
化学信息
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CAS Number1313019-65-6
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分子量431.8
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分子式C21H13ClF3N3O2
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 250 mg/mL (578.97 mM)
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SMILESN#Cc(cc1)ccc1Oc(cc1)ccc1NC(Nc(cc1)cc(C(F)(F)F)c1Cl)=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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.
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