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目錄:愛必信(上海)生物科技有限公司>>生化試劑>>小分子化合物>> abs810374SB525334

SB525334

  • SB525334
參考價419
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參考價:¥ 419

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  • absin 品牌
  • abs810374 型號
  • 生產商 廠商性質
  • 上海市 所在地
規(guī)格

2mg

屬性

CAS:356559-20-1 純度:>98% 分子量:343.42 分子式:C21H21N5 供貨周期:現貨 規(guī)格:2mg 貨號:abs810374 應用領域:化工,生物產業(yè),農林牧漁,制藥/生物制藥,綜合 主要用途:SB-525334;SB 525334;TGF-β RI Kinase Inhi

>
規(guī)格
2mg419元999mg可售

更新時間:2025-11-11 14:39:45瀏覽次數:1115評價

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CAS 356559-20-1 純度 >98%
分子量 343.42 分子式 C21H21N5
供貨周期 現貨 規(guī)格 2mg
貨號 abs810374 應用領域 化工,生物產業(yè),農林牧漁,制藥/生物制藥,綜合
主要用途 SB-525334;SB 525334;TGF-β RI Kinase Inhi
SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM, is 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.

SB525334

產品描述
描述

SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM, is 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.

純度
>98%
儲存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
別名
SB-525334;SB 525334;TGF-β RI Kinase Inhibitor VIII
外觀
yellow Powder
可溶性/溶解性
1eq. HCl : 34.3 mg/mL (100 mM)
DMSO : 34.3 mg/mL (100 mM)
生物活性
靶點
TGFβR1(ALK5)
In vitro(體外研究)
SB 525334 shows no inhibition in the enzymes ALK2, 3, and 6, with IC50 values > 10 μM. SB 525334 blocks phosphorylation induced by TGF-β1 and nuclear translocation of Smad2/3 in renal proximal tubule cells. SB 525334 also inhibits the increased mRNA expression levels of plasminogen activator inhibitor-1 (PAI-1) and procollagen α1(I) induced by TGF-β1 in A498 renal epithelial carcinoma cells at 1 μM). SB 525334 (1 μM) attenuates the heightened sensitivity to TGF-β1 exhibited by pulmonary artery smooth muscle cells (PASMCs) from patients with familial forms of idiopathic pulmonary arterial hypertension (PAH).
In vivo(體內研究)
SB 525334 (10 mg/kg/day) decreases the renal mRNA levels of PAI-1, procollagen α1(I), and procollagen α1(III) in a nephritis-induced renal fibrosis rat model. Furthermore, PAN-induced proteinuria is significantly inhibited by SB 525334 (10 mg/kg/day). SB 525334 may also be efficacious in mesenchymal tumors. SB 525334 (10 mg/kg/day) significantly decreases uterine mesenchymal tumor incidence, multiplicity, and size in Eker rats. SB 525334 significantly reverses pulmonary arterial pressure and inhibits right ventricular hypertrophy in a rat model of PAH. This is revealed by a significant reduction in pulmonary arteriole muscularization induced by monocrotaline (used to induce PAH) after treatment with SB 525334 (3 or 30 mg/kg). In a Bleomycin-induced pulmonary fibrosis mice model, SB 525334 (10 mg/kg or 30 mg/kg) attenuates the histopathological alterations in the lung, and significantly decreased mRNA expression of Type I and III procollagen and fibronectin. SB 525334 also attenuates Smad2/3 nuclear translocation, myofibroblast proliferation, deposition of Type I collagen, and decreases CTGF-expressing cells.
研究領域
研究領域
CancerCancer Metabolism
Drug DiscoverySmall Molecule DrugLead Compound Discovery
溫馨提示:本產品僅作科研實驗使用,不支持臨床等研究


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