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LY2109761

71 Cited Publications
고객리뷰

Based on 71 publication(s) in Google Scholar

LY2109761 is an orally active, selective TGF-β receptor type I/II inhibitor with Kis of 38 nM and 300 nM, respectively.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

  • Purity: 99.72%
  • CAS No.: 700874-71-1
  • 화학식: C26H27N5O2
  • 분자량:441.52
  • 보관:
    Powder   -20°C, 3 years , 4°C, 2 years ; In solvent   -80°C, 1 year , -20°C, 6 months
  • LY2109761 Chemical Structure
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • LY2109761 Chemical Structure
    LY2109761 Chemical Structure
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
  • Experimental Validation Results for LY2109761
CAS No.: 700874-71-1
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  • LY2109761 Chemical Structure
    LY2109761 Chemical Structure
    1/16
  • 1/16

    LY2109761 purchased from MedChemExpress. Usage Cited in: Biochim Biophys Acta Mol Basis Dis. 2018 Nov;1864(11):3824-3836. [Abstract]

    Customer Validation
     LY2109761 at 100 nM, 10 μM, or 50 μM is added for 30 min to block TGFβR1/2 prior to TGF-β1-treatment, then proteins are collected, and the levels of Sphk2, fibronectin, and α-SMA are detected by Western blotting.

  • 1/16

    LY2109761 purchased from MedChemExpress. Usage Cited in: Mol Immunol. 2018 Nov:103:173-181. [Abstract]

    Customer Validation
     TRPM7 mRNA and protein expressions are effectively suppressed by LY2109761 and SIS3 in ASMCs compared with those in 10 ng/mL TGF-β1-stimulated cells.

  • 1/16

    LY2109761 purchased from MedChemExpress. Usage Cited in: Cell Biol Int. 2017 Sep;41(9):960-968. [Abstract]

    Customer Validation
     The phosphorylation level of Smad2 is significantly inhibited by LY2109761. The M2 macrophage-induced increase of α-SMA and decrease of E-cadherin and CK-18 are inhibited by LY2109761.

  • 1/16

    LY2109761 purchased from MedChemExpress. Usage Cited in: J Hepatol. 2015 Oct;63(4):863-73. [Abstract]

    Customer Validation
     Blocking the TGF-beta and ERK signalling effectively inhibits EDIL3 mediated angiogenesis and invasion. Western blotting analysis of the expression of p-ERK and p-Smad2 in DMSO- and VX-11e or LY2109761-treated HuH7-p-lenti-EDIL3 cells. GAPDH is used as a loading control.

  • 1/16

    LY2109761 purchased from MedChemExpress. Usage Cited in: Int J Mol Med. 2015 Jun;35(6):1667-74. [Abstract]

    Customer Validation
     Inhibition of the TGF-β1/Smad2 pathway decreases H2O2-induced human umbilical vein endothelial cell (HUVEC) apoptosis, but not oxidative stress. Western blot analysis is performed to determine protein expression in the HUVECs in the control, model, AST Ⅳ and LY2109761 groups.

  • LY2109761