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目錄:MedChemExpress LLC>>生化試劑>> Nintedanib | MCE

Nintedanib | MCE
  • Nintedanib | MCE
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更新時(shí)間:2023-06-19 09:21:54瀏覽次數(shù):133評(píng)價(jià)

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CAS 656247-17-5 純度 99.85%
分子量 539.62 分子式 C??H??N?O?
供貨周期 現(xiàn)貨 規(guī)格 5 mg
貨號(hào) HY-50904 應(yīng)用領(lǐng)域 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥
Nintedanib | MCENintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for <b>VEGFR1/2/3</b>, <b>FGFR1/2/3</b> and <b>PDGFRα/β</b> with <b>IC<sub>50</sub></b>s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.

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Nintedanib

CAS No. : 656247-17-5

產(chǎn)品活性:Nintedanib (BIBF 1120) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50s of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM, respectively.

研究領(lǐng)域:Protein Tyrosine Kinase/RTK

作用靶點(diǎn):PDGFR  |  VEGFR  |  FGFR

In Vitro: Nintedanib (BIBF 1120) binds to the ATP-binding site in the cleft between the amino and carboxy terminal lobes of the kinase domain. Nintedanib (BIBF 1120) inhibits proliferation of PDGF-BB stimulated BRPs with EC50 of 79 nM in cell assays. Nintedanib (BIBF 1120) (100 nM) blocks activation of MAPK after stimulation with 5% serum plus PDGF-BB. Nintedanib (BIBF 1120) prevents PDGF-BB stimulated proliferation with an EC50 of 69 nM in cultures of human vascular smooth muscle cells (HUASMC).

In Vivo: Nintedanib (BIBF 1120) (25-100 mg/kg daily p.o.) is highly active in all tumor models, including human tumor xenografts growing in nude mice and a syngeneic rat tumor model. This is evident in the magnetic resonance imaging of tumor perfusion after 3 days, reducing vessel density and vessel integrity after 5 days, and profound growth inhibition. Nintedanib (BIBF 1120) is orally available and displays encouraging efficacy in in vivo tumor models while being well tolerated.

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