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SC-43

SC-43

中文名稱(chēng)SC-43
中文同義詞化合物SC-43;1-(4-氯-3-(三氟甲基)苯基)-3-(3-(4-氰基苯氧基)苯基)脲;化合物SC-43,10 MM DMSO 溶液
英文名稱(chēng)SC-43
英文同義詞1-(4-chloro-3-(trifluoromethyl)phenyl)-3-(3-(4-cyanophenoxy)phenyl)urea;SC-43;Urea, N-[4-chloro-3-(trifluoromethyl)phenyl]-N'-[3-(4-cyanophenoxy)phenyl]-;antiproliferative,Inhibitor,SC-43,SHP-1,PTPN6,Phosphatase,Apoptosis,caspase-3,SC 43,anti-fibrotic,p-STAT3,anticancer,orally,SC43,PARP,STAT,inhibit;SC-43, 10 mM in DMSO
CAS號(hào)1400989-25-4
分子式C21H13ClF3N3O2
分子量431.8
EINECS號(hào)
相關(guān)類(lèi)別
Mol文件1400989-25-4.mol
結(jié)構(gòu)式SC-43 結(jié)構(gòu)式

SC-43 性質(zhì)

沸點(diǎn)462.0±45.0 °C(Predicted)
密度1.46±0.1 g/cm3(Predicted)
儲(chǔ)存條件Store at -20°C
溶解度二甲基亞砜:250 mg/ml(578.97 mM)
形態(tài)固體
酸度系數(shù)(pKa)12.92±0.70(Predicted)
顏色白色至米白色

SC-43 用途與合成方法

SC-43 是索拉非尼sorafenib的衍生物,是一種 Src-homology protein tyrosine phosphatase-1 (SHP-1/PTPN6) 的激動(dòng)劑,可減少肝纖維化。SC-43 可減少 p-STAT3 并誘導(dǎo)凋亡,具有抗腫瘤的活性。
TargetValue
SHP-1
()
STAT3
()

SC-43 (0-10 μM; 24-72 hours; HuCCT-1, KKU-100, and CGCCA cells) treatment reveals the anti-proliferative effects in cholangiocarcinoma (CCA) cell lines in a dose-dependent manner after treating 24, 48 and 72 hours respectively.
SC-43 (0-10 μM; 24 hours; HuCCT-1, KKU-100, and CGCCA cells) treatment shows increased sub-G1 cells and G2-M arrest, indicating SC-43 induced differential apoptotic effects in these cell lines.
SC-43 (0-10 μM; 24 hours; HuCCT-1, KKU-100, and CGCCA cells) treatment demonstrates significant increase in cleaved caspase-3 and PARP level.
SC-43 activates SH2 domain-containing phosphatase 1 (SHP-1) activity, leading to p-STAT3 and downstream cyclin B1 and Cdc2 downregulation. SC-43 augments SHP-1 activity by direct binding to N-SH2 and relief of its autoinhibition.

Cell Viability Assay

Cell Line: HuCCT-1, KKU-100, and CGCCA cells
Concentration: 0 μM, 0.25 μM, 0.5 μM, 0.75 μM, 1 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 24 hours, 48 hours, 72 hours
Result: Revealed the anti-proliferative effects in CCA cell lines in a dose-dependent manner after treating 24, 48 and 72 hours respectively.

Cell Cycle Analysis

Cell Line: HuCCT-1, KKU-100, and CGCCA cells
Concentration: 0 μM, 1 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 24 hours
Result: Showed increased sub-G1 cells and G2-M arrest.

Western Blot Analysis

Cell Line: HuCCT-1, KKU-100, and CGCCA cells
Concentration: 0 μM, 1 μM, 2.5 μM, 5 μM, 10 μM
Incubation Time: 24 hours
Result: Demonstrated significant increase in cleaved caspase-3 and PARP level.

SC-43 (10-30 mg/kg; oral gavage; daily; for 23 days; male NCr athymic nude mice) treatment exhibits xenograft tumor growth inhibition, p-STAT3 reduction and SHP-1 activity elevation.

Animal Model: Male NCr athymic nude mice (5-7 weeks of age) injected with HuCCT-1 cells
Dosage: 10 mg/kg or 30 mg/kg
Administration: Oral gavage; daily; for 23 days
Result: Exhibited xenograft tumor growth inhibition, p-STAT3 reduction and SHP-1 activity elevation.

安全信息

MSDS信息

更新日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2025/02/08HY-136657SC-431400989-25-41 mg952元
2025/02/08HY-136657SC-43
SC-43
1400989-25-45mg2475元

SC-43 上下游產(chǎn)品信息

"SC-43"相關(guān)產(chǎn)品信息
SC75741 SC-1 5-(4-氯苯基)-1-(4-甲氧基苯基)-3-(三氟甲基)-1H-吡唑 4-(5-(4-氯苯基)-3-(三氟甲基)-1H- ALPHA,ALPHA-二苯基-4-[(3-吡啶亞甲基)氨基]-1-吡嗪戊腈
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