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ML-385

CAS No. 846557-71-9

ML-385 ( ML 385 | ML385 )

产品货号. M16145 CAS No. 846557-71-9

一种一流的 NRF2 小分子抑制剂,可与 NRF2 的 Neh1 DNA 结合域结合(IC50=1.9 uM)并抑制下游靶基因表达。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥588 有现货
10MG ¥1017 有现货
25MG ¥1814 有现货
50MG ¥2539 有现货
100MG ¥3591 有现货
200MG ¥5211 有现货
500MG ¥7974 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥652 有现货

生物学信息

  • 产品名称
    ML-385
  • 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
    一种一流的 NRF2 小分子抑制剂,可与 NRF2 的 Neh1 DNA 结合域结合(IC50=1.9 uM)并抑制下游靶基因表达。
  • 产品描述
    A first-in-class small molecule inhibitor of NRF2 that binds to Neh1 DNA binding domain of NRF2 (IC50=1.9 uM) and inhibits the downstream target gene expression; blocks the binding of the NRF2-MAFG complex to the ARE sequence in the promoter and reduces transcriptional activity; inhibits NRF2 signaling in lung cancer cells with KEAP1 mutations, shows selective cytotoxicity in NSCLC cells with KEAP1 mutations and potentiates the toxicity chemotherapy drugs; shows anti-tumor activity in NSCLC both as a single agent and in combination with carboplatin in preclinical models of NSCLC.Lung Cancer Preclinical(In Vitro):ML385 interacts with NRF2 and affects the DNA binding activity of the NRF2-MAFG protein complex. The addition of ML385 decreases anisotropy in a dose-dependent manner, with an IC50 of 1.9 μM. A dose-dependent reduction in the NRF2 transcriptional activity is observed and the maximum inhibitory concentration is 5 μM by ML385. Treatment with ML385 leads to a significant reduction in NRF2 and downstream target gene expression selectively in KEAP1 mutant H460 cells. ML385 selectively affects the colony forming ability or growth of lung cancer cells with gain of NRF2 function.(In Vivo):ML385 in combination with carboplatin leads to a significant reduction in tumor cell proliferation, demonstrated by fewer Ki-67 positive cells. Tumor samples treated with ML385 show a significant reduction in NRF2 protein level and its downstream target genes.ML385 (intraperitoneal injection; 30 mg/kg; 7 days) weakens the therapeutic effects of MSC-Exo on inflammation-induced astrocytic activation in mice, and reduces reactive astrogliosis, NF-κB deactivation.
  • 体外实验
    ——
  • 体内实验
    Animal Model:8-week-old C57B/6 male mice Dosage:30 mg/kg; 7 days Administration:Intraperitoneal injection Result:Reversed inhibition of MSC-Exo on hippocampal astrocytic activation in vivo.
  • 同义词
    ML 385 | ML385
  • 通路
    Nuclear Receptor/Transcription Factor
  • 靶点
    Keap1-Nrf2
  • 受体
    Nrf2
  • 研究领域
    Cancer
  • 适应症
    Lung Cancer

化学信息

  • CAS Number
    846557-71-9
  • 分子量
    507.6459
  • 分子式
    C31H29N3O2S
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO: ≥ 30 mg/mL
  • SMILES
    O=C(NC1=NC(C2=CC3=C(N(C(C4=CC=CC=C4C)=O)CC3)C=C2)=C(C)S1)CC5=CC=C(OCO6)C6=C5
  • 化学全称
    1,3-Benzodioxole-5-acetamide, N-[4-[2,3-dihydro-1-(2-methylbenzoyl)-1H-indol-5-yl]-5-methyl-2-thiazolyl]-

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. Singh A, et al. ACS Chem Biol. 2016 Nov 18;11(11):3214-3225.
产品手册
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