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1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea

SKU: orb1940396

Description

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.

Images & Validation

Key Properties

CAS Number1313019-65-6
MW431.8
Purity>98% (HPLC)
FormulaC21H13ClF3N3O2
SMILESN#Cc(cc1)ccc1Oc(cc1)ccc1NC(Nc(cc1)cc(C(F)(F)F)c1Cl)=O
TargetApoptosis
SolubilityIn Vitro: DMSO : 250 mg/mL (578.97 mM)

Bioactivity

In Vivo
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.
In Vitro
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 Assay 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: 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 hours. Result: Showed downregulation of p-STAT3 and its downstream proteins cyclin D1 and survivin in a dose-dependent manner in breast cancer cell lines.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

SC-1

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  • 1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea [orb1305935]

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1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea (orb1940396)

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200 mg
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5 mg
$ 380.00
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$ 580.00
25 mg
$ 1,020.00
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$ 1,460.00
100 mg
$ 1,930.00