1. Signaling Pathways
  2. Cytoskeleton
  3. Claudin

Claudin 

Claudins are a family of transmembrane proteins, are the most important components of the tight junctions (zonulae occludentes). They have four transmembrane domains, with the N-terminus and the C-terminus in the cytoplasm. Claudin expression and functions are regulated at multiple levels and by diverse mechanisms. Delocalization of claudins from membrane appears to be common among the transformed cells. Constitutive activation of Ras or Ras-mediated signaling pathway/s is one of the initial steps during tumorigenesis that is causatively associated with neoplastic transformation. Importantly, claudins are expressed in the epithelial cells and in a tissue-specific manner and changes among claudin family members in cancer follow tissue-specific and sometimes contrasting pattern. Thus, claudin family of proteins may hold the potential cue to the heterogeneity among the tumors of epithelial origin and beyond being useful markers may also help provide therapeutic opportunities suited for specific cancer type[1].

Claudin 相关产品 (9):

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-N2468
    Xylobiose

    木二糖

    Inhibitor ≥98.0%
    Xylobiose (1,4-β-D-Xylobiose; 1,4-D-Xylobiose) 是一种口服有效的 Claudin 2/CLDN2 抑制剂及 HSP27 诱导剂。Xylobiose 通过调节肠道屏障功能及糖脂代谢相关信号通路发挥作用。Xylobiose 抑制 CLDN2 表达以减少肠道通透性,诱导 HSP27 增强细胞保护,同时调控 miR-122a/miR-33a 轴以抑制肝脏脂质合成、改善胰岛素抵抗。Xylobiose 可强化肠道屏障完整性、降低血糖和血脂水平、减轻氧化应激及炎症反应。Xylobiose 可用于 2 型糖尿病及代谢综合征的研究。
    Xylobiose
  • HY-W014507
    9,10-Phenanthrenequinone

    菲醌

    Inhibitor 99.95%
    9,10-Phenanthrenequinone 是 claudin-5/CLDN5 的抑制剂,通过 NO 合酶/ROS 依赖机制引发细胞凋亡。9,10-Phenanthrenequinone 还促进 Caspase 激活和 DNA 断裂,并降低 CLDN5 表达和蛋白酶体蛋白水解来促进内皮细胞屏障功能障碍。
    9,10-Phenanthrenequinone
  • HY-171152A
    NSC 357754 dihydrochloride Inhibitor 98.01%
    NSC 357754 dihydrochloride 是一种 Claudin 的抑制剂。NSC 357754 dihydrochloride 能够增加细胞跨上皮电阻和降低特定阳离子通透性。NSC 357754 dihydrochloride 可用于 Claudin-2 和或 Claudin-15 介导的肠道疾病的研究。
    NSC 357754 dihydrochloride
  • HY-N7635
    Oleanolic acid 28-O-β-D-glucopyranoside Activator 99.42%
    Oleanolic acid 28-O-β-D-glucopyranoside (β-D-Glucopyranosyl oleanolate) 是一种具有口服活性的五环三萜类化合物。Oleanolic acid 28-O-β-D-glucopyranoside 具有抗炎作用。Oleanolic acid 28-O-β-D-glucopyranoside 在溃疡性结肠炎模型中,可抑制炎症反应、增强肠道上皮屏障功能、调节肠道微生物群落,作用机制与 PI3K-AKTMAPK 信号通路相关。Oleanolic acid 28-O-β-D-glucopyranoside 可用于结肠炎等疾病的研究。
    Oleanolic acid 28-O-β-D-glucopyranoside
  • HY-171152
    NSC 357754 Inhibitor
    NSC 357754 是一种 Claudin 的抑制剂。NSC 357754 能够增加细胞跨上皮电阻和降低特定阳离子通透性。NSC 357754 可用于 Claudin-2 和或 Claudin-15 介导的肠道疾病的研究。
    NSC 357754
  • HY-P991200
    OM-7D3-B3 Inhibitor
    OM-7D3-B3 是一种单克隆抗体,靶向人紧密连接蛋白 1 (CLDN1) (Kd= 4 nM)。OM-7D3-B3 阻断 CLDN1 参与丙型肝炎病毒 (HCV) 进入细胞的过程。OM-7D3-B3 有望用于 HCV 感染的研究。
    OM-7D3-B3
  • HY-P991163
    Tixentamig Inhibitor
    Tixentamig 是一种双特异性单克隆抗体,靶向人源 CD3 εCLDN18 (claudin 18)。Tixentamig 有望用于癌症的研究。
    Tixentamig
  • HY-P991140
    Garetatug Ligand
    Garetatug 是一种人源化单克隆抗体,靶向人 CLDN18 (claudin-18)。Garetatug 特异性结合 CLDN18,干扰相关细胞信号通路,发挥抗肿瘤活性。
    Garetatug
  • HY-P991143
    Ixotatug Ligand
    Ixotatug 是一种单克隆抗体,靶向人 CLDN6 (claudin-6)。Ixotatug 特异性结合 CLDN6,干扰肿瘤细胞相关信号通路,发挥抗肿瘤活性。Ixotatug 有望用于癌症的研究。
    Ixotatug