C188-9,432001-19-9

C188-9,432001-19-9

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  • ¥1000 - 5922
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-112288
  • 2025年12月05日
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    • 详细信息
    • 询价记录
    • 技术资料
    • 保存条件

      4°C, protect from light

    • 英文名

      TTI-101

    • 库存

      货期:1-2天

    • 供应商

      MedChemExpress LLC

    • CAS号

      432001-19-9

    • 规格

      10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg

    规格:10 mM * 1 mL产品价格:¥1100.0
    规格:5 mg产品价格:¥1000.0
    规格:10 mg产品价格:¥1245.0
    规格:25 mg产品价格:¥2700.0
    规格:50 mg产品价格:¥4230.0
    规格:100 mg产品价格:¥5922.0

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    C188-9

    CAS No. : 432001-19-9

    MCE 国际站:C188-9

    产品活性:C188-9 (TTI-101) 是 Stat3 的抑制剂,其 Kd 值为 4.7 nM。C188-9 抑制 G-CSF 诱导的 STAT3 激活和 STAT3 依赖性基因表达。C188-9 诱导 AML 细胞系和原代标本凋亡,抑制原代 AML 细胞集落形成。

    研究领域:JAK/STAT Signaling  |  Stem Cell/Wnt  |  Apoptosis

    作用靶点:STAT  |  Apoptosis

    In Vitro: C188-9 is a Stat3 inhibitor, with a Kd of 4.7 nM. The IC50s of C188-9 to inhibit Stat3 activation in AML cell lines are in the range of 4-7 μM, and in primary AML samples the IC50s are in the range of 8-18 μM. For apoptosis studies, AML cell lines and primary samples are treated for 24 hours with C188-9, then apoptotic cells are quantified by FACS analysis for annexin V-labeled cells. The EC50s for apoptosis induction are quite variable, ranging from 6 μM to over 50 μM.

    In Vivo: Of the approximately 13,528 discernible genes, levels of 37 gene transcripts are altered by C188 (17 down and 20 up-regulated, fdr <0.01, fold change≥1.5), of which 7 are known STAT3 gene targets. In comparison, C188-9 affects a much greater number of genes involved in oncogenesis (384 total, 95 down- and 289 up-regulated), including 76 genes previously reported as regulated by STAT3 (38 down-regulated and 38 up-regulated). Among the 38 genes previously shown to be upregulated by STAT3, 24 (63%) genes are downregulated by C188-9 treatment, as expected. Additionally, 10 more genes downregulated by C188-9 (fdr <0.01, fold change≥1.5) that previously are shown to be upregulated by STAT1. Thus, 40 of 48 (83.3%) genes downregulated by C188-9 previously are shown to be positively regulated by STAT1, including sixteen genes shown to be co-regulated by STAT3 and STAT1. This analysis raises the possibility that the effect of C188-9 on gene transcript levels in HNSCC tumors is mediated by its effects on both STAT3 and STAT1.

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