• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Loureirin B

CAS No. 119425-90-0

Loureirin B ( Loureirin B | LR-B | L B | LRB )

产品货号. M17868 CAS No. 119425-90-0

Loureirin B可以通过调节MMPs和TIMPs水平下调纤维化相关分子的表达,抑制疤痕成纤维细胞增殖,抑制TGF-β1诱导的纤维化,其中TGF-β1/Smad2/3通路可能参与其中。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1169 有现货
10MG ¥1729 有现货
25MG ¥2762 有现货
50MG ¥4120 有现货
100MG ¥5625 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥1292 有现货

生物学信息

  • 产品名称
    Loureirin B
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Loureirin B可以通过调节MMPs和TIMPs水平下调纤维化相关分子的表达,抑制疤痕成纤维细胞增殖,抑制TGF-β1诱导的纤维化,其中TGF-β1/Smad2/3通路可能参与其中。
  • 产品描述
    Loureirin B can downregulate the expression of fibrosis-related molecules by regulating MMPs and TIMPs levels, inhibit scar fibroblast proliferation and suppress TGF-β1-induced fibrosis, during which TGF-β1/Smad2/3 pathway is likely involved.
  • 体外实验
    Loureirin B enhances the relative mRNA level of Pdx-1 and MafA. Loureirin B (1, 0.1, and 0.01?μM) increases insulin secretion in Ins-1 cells. Loureirin B (0.01?μM) almost causes no toxicity on cells. Loureirin B improves the level of expressions of MafA and Pdx-1 and ATP level. Loureirin B inhibits the KATP current but increases the [Ca2+]i level in Ins-1 cells. Loureirin B inhibits the expression of Col1 and FN, as well as the TGF-β1-mediated up regulation of p-JNK. Loureirin B also inhibits the up regulation of p-ERK that is induced by TGF-β1. Moreover, Loureirin B inhibits the contraction of TGF-β1-stimulated fibroblasts through the down regulation of p-ERK and p-JNK. However, Loureirin B does not suppress the up regulation of p-p38 that is induced by TGF-β1. Loureirin B downregulates both mRNA and protein levels of type I collagen, type III collagen and α-smooth muscle actin in a dose dependent manner in HS fibroblasts. Loureirin B also suppresses fibroblast proliferative activity and redistributes cell cycle, but does not affect cell apoptosis.
  • 体内实验
    Loureirin B significantly improves the arrangement and deposition of collagen fibres, decreases protein levels of ColI, ColIII and α-SMA and suppresses myofibroblast differentiation and scar proliferative activity, in a rabbit ear scar model. Loureirin B effectively inhibits TGF-β1-induced upregulation of ColI, ColIII and α-SMA levels, myofibroblast differentiation and the activation of Smad2 and Smad3, in NS fibroblasts.
  • 同义词
    Loureirin B | LR-B | L B | LRB
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    DNA/RNA Synthesis
  • 受体
    Others
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    119425-90-0
  • 分子量
    316.35
  • 分子式
    C18H20O5
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 150 mg/mL; 474.16 mM
  • SMILES
    COc1cc(c(c(c1)OC)CCC(=O)c1ccc(cc1)O)OC
  • 化学全称
    1-(4-hydroxyphenyl)-3-(2,4,6-trimethoxyphenyl)propan-1-one

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1. Bai X, et al. Loureirin B inhibits fibroblast proliferation and extracellular matrix deposition in hypertrophic scar via TGF-β/Smad pathway. Exp Dermatol. 2015 May;24(5):355-60.
产品手册
关联产品
  • Dmt-2fluoro-da(bz) a...

    Dmt-2'fluoro-da(bz) amidite,一种均一修饰的 2'-脱氧-2'-氟代硫代磷酸酯寡核苷酸,是抗核酸酶的反义化合物,对 RNA 靶标具有很高的亲和力和特异性。Dmt-2'fluoro-da(bz) amidite 也是 5'-DMT-3'-亚磷酰胺合成的中间体。

  • Elinafide

    Elinafide, a dinaphthylimide cytotoxic agent, is a DNA-targeted anticancer agent that has shown antitumor activity in in vitro and in vivo assays.

  • T863

    T-863(DGAT-1抑制剂)是一种口服活性、选择性和有效的DGAT1(酰基辅酶A:二酰基甘油酰基转移酶1)抑制剂,与DGAT1的酰基辅酶A结合位点相互作用,并抑制细胞中三酰基甘油的合成。