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          目錄:MedChemExpress LLC>>信號通路>> Lucitanib | 德立替尼 | MedChemExpress (MCE)

          Lucitanib | 德立替尼 | MedChemExpress (MCE)
          • Lucitanib | 德立替尼 | MedChemExpress (MCE)
          參考價 1210
          具體成交價以合同協(xié)議為準
          參考價 1210
          具體成交價以合同協(xié)議為準
          • 品牌 MedChemExpress (MCE)
          • 型號
          • 廠商性質(zhì) 生產(chǎn)商
          • 所在地 國外
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          更新時間:2024-01-10 11:28:15瀏覽次數(shù):149評價

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          CAS 1058137-23-7 純度 98.94%
          分子量 443.49 分子式 C??H??N?O?
          供貨周期 現(xiàn)貨 規(guī)格 10 mM * 1 mL
          貨號 HY-15391 應用領域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
          Lucitanib (E-3810) 是 VEGFR 和 FGFR 的雙重抑制劑,有效和選擇性地抑制VEGFR1,VEGFR2,VEGFR3,F(xiàn)GFR1,F(xiàn)GFR2,IC50分別為7 nM,25 nM,10 nM,17.5 nM,82.5 nM。

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          Lucitanib

          CAS No. : 1058137-23-7

          MCE 國際站:Lucitanib

          產(chǎn)品活性:Lucitanib (E-3810) 是 VEGFRFGFR 的雙重抑制劑,有效和選擇性地抑制VEGFR1,VEGFR2,VEGFR3,FGFR1FGFR2,IC50分別為7 nM,25 nM,10 nM,17.5 nM,82.5 nM。

          研究領域:Protein Tyrosine Kinase/RTK

          作用靶點:VEGFR  |  FGFR

          In Vitro: Consistent with the inhibitory activity of VEGFR and FGFR auto-phosphorylation, Lucitanib potently inhibits VEGF and bFGF-stimulated HUVEC proliferation with IC50 of 40 and 50 nM, respectively. Besides, Lucitanib (E-3810) also inhibits CSF-1R with IC50 of 5 nM. Lucitanib potently inhibits FGFR2 activity (Ki<0.05 μM), follows by PDGFRα activity (Ki=0.11 μM). The Ki values obtained for DDR2, LYN, CARDIAK, CSBP (2), EPHA2, and YES range between 0.26 and 8 μM.

          In Vivo: Lucitanib (E-3810), at oral dosing of 20 mg/kg for 7 consecutive days, completely inhibits (P<0.01) the bFGF induced angiogenic response compare with the response in vehicle-treated mice. Lucitanib (E-3810) shows a broad spectrum of activity, being active in all the xenografts tested (HT29 colon carcinoma, A2780 ovarian carcinoma, A498, SN12K1, and RXF393 renal carcinomas) with dose-dependent inhibition of tumor growth. E-3810 significantly delays growth during treatment, but tumors resume their growth when treatment is suspended; in a few cases, tumor regression is observed. The activity of Lucitanib (E-3810) given at the doses of 15 mg/kg is tested on MDA-MB-231 breast cancer transplanted subcutaneously, at a late stage, when tumor masses reach 350 to 400 mg. This tumor xenograft is very sensitive to Lucitanib (E-3810), with complete tumor stabilization lasting throughout the 30-day treatment. As in other tumor models, tumors re-grow after withdrawal of Lucitanib (E-3810) at a rate similar to control tumors.

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