1. Signaling Pathways
  2. JAK/STAT Signaling
    Stem Cell/Wnt
  3. STAT


STAT is a family of cytoplasmic protein that regulates many aspects of growth, survival and differentiation in cells. The transcription factors of this family are activated by Janus kinase and dysregulation of this pathway is frequently observed in primary tumours and leads to increased angiogenesis, enhanced survival of tumours and immunosuppression. Gene knockout studies have provided evidence that STAT proteins are involved in the development and function of the immune system and play a role in maintaining immune tolerance and tumour surveillance. STAT proteins were originally described as latent cytoplasmic transcription factors that require phosphorylation for nuclear retention. The unphosphorylated STAT proteins shuttle between cytosol and the nucleus waiting for its activation signal. Once the activated transcription factor reaches the nucleus, it binds to consensus DNA-recognition motif called gamma-activated sites (GAS) in the promoter region of cytokine-inducible genes and activates transcription of these genes.

STAT Isoform Specific Products:

  • STAT3

  • STAT5

  • STAT6

STAT 相关产品 (46):

Cat. No. Product Name Effect Purity
  • HY-12000
    AG-490 Inhibitor 99.84%
  • HY-13818
    Stattic Inhibitor >98.0%
    Stattic是有效的 STAT3 活化和二聚化的抑制剂。
  • HY-15146
    NSC 74859 Inhibitor 99.50%
    NSC 74859是选择性的 Stat3 抑制剂,IC50 为86±33 μM。
  • HY-100614
    AS1517499 Inhibitor 99.17%
    AS1517499 是有效的 STAT6 抑制剂,IC50 为 21 nM。
  • HY-101853
    STAT5-IN-1 Inhibitor >98.0%
    STAT5-IN-1是 STAT5 的抑制剂,对 STAT5β 亚型的 IC50 值为 47 μM。
  • HY-113573
    Protosappanin A 98.88%
    Protosappanin A (PTA),是一种免疫制剂,是从 Caesalpinia sappan L 中分离得到的一种主要联苯化合物,通过下调 JAK2STAT3 的磷酸化,抑制 JAK2/STAT3 依赖的炎症通路。
  • HY-100544
    FLLL32 Inhibitor 99.78%
    FLLL32,一种姜黄素的合成类似物,是 JAK2/STAT3 的双重抑制剂,具有抗肿瘤癌活性。
  • HY-100753
    STAT3-IN-1 Inhibitor
    STAT3-IN-1 (compound 7d) 是强效的、选择性的、口服有效的STAT3 的抑制剂,其在HT29 和MDA-MB 231 细胞中的 IC50 值分别为1.82 μM 和2.14 μM。STAT3-IN-1 (compound 7d) 可诱导肿瘤细胞凋亡。
  • HY-N0174
    Cryptotanshinone Inhibitor 98.51%
    Cryptotanshinone是从丹参的根中提取的天然化合物,具有抗肿瘤活性。 Cryptotanshinone抑制 STAT3IC50 为4.6 μM。
  • HY-112288
    C188-9 Inhibitor 98.11%
    C188-9 是 Stat3 的抑制剂,其 Kd 值为 4.7 nM。
  • HY-15312
    WP1066 Inhibitor 99.67%
    WP1066 是一种新颖的 JAK2STAT3 抑制剂,对 STAT5 和 ERK1/2 也起作用,但对 JAK1 和 JAK3 没有影响。
  • HY-14944
    Homoharringtonine Inhibitor 99.96%
    Homoharringtonine (Omacetaxine mepesuccinate;HHT) 是具有抗肿瘤特性的细胞毒性生物碱,其通过抑制翻译延长来起作用。
  • HY-100493
    BP-1-102 Inhibitor 99.23%
    BP-1-102 是有口服活性的转录因子 Stat3 的小分子抑制剂,其 IC50 值为 6.8 μM。
  • HY-13919
    Napabucasin Inhibitor >98.0%
    Napabucasin 是 STAT3 的抑制剂,抑制癌症干细胞活性。
  • HY-10074
    TPCA-1 Inhibitor 99.54%
    TPCA-1 是一种有效,选择性的 IKK-2 抑制剂,IC50 值为 17.9 nM。TPCA-1 也是STAT3 磷酸化、DNA结合以及反式激活的有效抑制剂。
  • HY-B0497
    Niclosamide Inhibitor
    Niclosamide是一种口服生物可利用的氯化水杨酰苯胺,具有驱虫和潜在的抗肿瘤活性。 Niclosamide可抑制 STAT3 ,在HeLa细胞中IC50 0.25 μM,并在无细胞试验中抑制DNA复制。
  • HY-N0751
    Scutellarin Inhibitor >98.0%
    Scutellarin 是从黄芩中分离到的黄酮类物质,在 HCC 细胞中,能够下调 STAT3/Girdin/Akt 信号通路,在破骨细胞中,能够抑制 RANKL 介导的 MAPK/NF-κB 信号通路。
  • HY-B0069
    Fludarabine Inhibitor 99.28%
    Fludarabine (F-ara-A; NSC 118218) 是 DNA 合成抑制剂,也抑制 STAT1 磷酸化。
  • HY-N0193
    Artesunate Inhibitor >98.0%
    Artesunate 是 STAT-3 和输出蛋白 1 (EXP1) 的抑制剂。
  • HY-16975
    SH-4-54 Inhibitor 98.19%
    SH-4-54是 STAT 的抑制剂,与 STAT3 和 STAT5 结合的 KDs 值分别为300,464 nM。
Isoform Specific Products

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Sorry. There is currently no product that acts on isoform together.

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