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A939572

    
99.8%

A939572

源葉(MedMol)
S81748 一鍵復(fù)制產(chǎn)品信息
1032229-33-6
C20H22ClN3O3
387.86
4-(2-氯苯氧基)-N-[3-[(甲胺基)羰基]苯基]-1-哌啶羧胺;(4-(2-chlorophenoxy)-N-(3-(methylcarbamoyl)-phenyl)piperidine-1-carboxamide); 4-(2-chlorophenoxy)-N-{3-[(methylamino)carbonyl]phenyl}piperidine-1-carboxamide; 4-(2-
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S81748-1mg
99.8% ¥305.00 >10 - - -
S81748-5mg
99.8% ¥920.00 >10 - - -
S81748-10mg
99.8% ¥1200.00 >10 - - -
S81748-50mg
99.8% ¥4900.00 >10 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關(guān)產(chǎn)品

產(chǎn)品介紹

A939572 是一種有效的、口服生物可利用的 stearoyl-CoA desaturase1 (SCD1) 的抑制劑,對 mSCD1 和 hSCD1 的 IC50值分別為 <4 nM 和 37 nM

產(chǎn)品描述: A939572 是一種有效的、口服生物可利用的 stearoyl-CoA desaturase1 (SCD1) 的抑制劑,對 mSCD1 和 hSCD1 的 IC50值分別為 <4 nM 和 37 nM
靶點: mSCD1(Cell-free assay):4 nM; hSCD1(Cell-free assay):37 nM;Dehydrogenase;?Stearoyl-CoADesaturase(SCD)
體外研究: A939572 demonstrates a significant dose-dependent decrease in proliferation in Caki1, A498, Caki2, and ACHN at day 5. In congruity with previous experimentation examining SCD1 lentiviral knockdown models, A939572 induces apoptosis confirmed by PARP cleavage via western blot analysis in all four cell lines. Treatment of ccRCC cells with A939572 induces Endoplasmic Reticulum Stress
體內(nèi)研究: When compared to the placebo control, all treatment groups (A939572, Tem, and Combo) exhibits decreased proliferation as marked by reduction in percent positivity of nuclear Ki67 staining, with the combinatorial group demonstrating the most significant decline. Combinatorial application of A939572 with temsirolimus synergistically inhibits tumor growth in vivo
細胞實驗: Cell lines: Caki1, A498, Caki2, ACHN ccRCC cells Concentrations: 75 nM Incubation Time: 24 h Method: In order to determine the mechanism of decreased proliferation and induction of cell death associated with loss of SCD1 activity in ccRCC cells, gene array analysis was performed with Caki1, A498, Caki2, and ACHN ccRCC cells treated for 24 hours with a 75nM dose of A939572 compared to DMSO control.
動物實驗: Animal Models: athymic nu/nu mice Dosages: 30 mg/kg Administration: Oral gavage
參考文獻: 1. Zhili Xin, et al. Discovery of piperidine-aryl urea-based stearoyl-CoA desaturase 1 inhibitors. Bioorg Med Chem Lett. 2008 Aug 1;18(15):4298-302. 2. Christina A von Roemeling, et al. Stearoyl-CoA desaturase 1 is a novel molecular therapeutic target for clear cell renal cell carcinoma. Clin Cancer Res. 2013 May 1;19(9):2368-80.
溶解性: Soluble  in  DMSO、Ethanol
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.578 ml 12.891 ml 25.782 ml
5 mM 0.516 ml 2.578 ml 5.156 ml
10 mM 0.258 ml 1.289 ml 2.578 ml
50 mM 0.052 ml 0.258 ml 0.516 ml
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參考文獻

質(zhì)檢證書(COA)

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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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