1. Signaling Pathways
  2. Membrane Transporter/Ion Channel
  3. CRM1

CRM1 (染色体维持蛋白1)

Chromosomal Maintenance 1; Exportin 1; XPO1

CRM1(染色体区域维护蛋白 1;Exportin 1;XPO1)是核转运蛋白 β 家族转运受体的成员,是一种重要的核蛋白输出受体,可识别疏水性、富含亮氨酸的核输出信号 (NES) 并跨 Ran-GTP 梯度转运靶蛋白。CRM1 参与多种货物蛋白的主动转运,包括转录因子、肿瘤抑制蛋白 (TSP) 和细胞周期调节剂,如 p53、p21、p27、核磷蛋白 1 (NPM1),以及 RNA 分子。

CRM1 异常上调可产生多种促癌后果。CRM1 上调将允许更多生长调节蛋白(如 c-myc 或 BCR-ABL)转运到细胞质中并激活下游信号,从而导致持续的细胞增殖。类似地,肿瘤抑制蛋白 (TSP),例如 Rb、p53、p21 或 p27,在输出时功能失活,从而消除了对不适当细胞生长的检查。类似的破坏也会发生在细胞凋亡、DNA 损伤修复、染色体稳定和血管生成等过程中,仅举几个例子。因此,抑制 CRM1 活性成为一个有吸引力的治疗靶点。

CRM1 (Chromosome region maintenance 1; Exportin 1; XPO1), a member of the karyopherin β family of transport receptors, is an important nuclear protein export receptor that recognizes hydrophobic, leucine-rich nuclear export signal (NES) and transports target proteins across a Ran-GTP gradient. CRM1 is involved in the active transport of a number of cargo proteins, including transcription factors, tumor suppressor proteins (TSPs), and cell-cycle regulators, such as p53, p21, p27, nucleophosmin 1 (NPM1), as well as RNA molecules.

Abnormal CRM1 upregulation can have several cancer-promoting consequences. Upregulation of CRM1 would allow more growth regulatory proteins, such as c-myc or BCR-ABL, to be transported into the cytoplasm and activate downstream signaling leading to sustained cell proliferation. Similarly, tumor suppressor proteins (TSPs), such as Rb, p53, p21, or p27, are functionally inactivated upon export, hence removing the check on inappropriate cell growth. Similar disruptions would occur in the processes of apoptosis, DNA damage repair, chromosomal stabilization, and angiogenesis, just to name a few examples. Hence, inhibition of CRM1 activity became an attractive therapeutic target.

Cat. No. Product Name Effect Purity Chemical Structure
  • HY-155972
    CRM1-IN-1 Inhibitor
    CRM1-IN-1 (Compound KL1) 是一种非共价 CRM1 抑制剂。CRM1-IN-1 诱导核 CRM1 降解(IC50: 0.27 μM)。CRM1-IN-1 抑制 CRM1 介导的核输出和细胞增殖,并触发结直肠癌细胞凋亡 (apoptosis)
    CRM1-IN-1
  • HY-170669
    PROTAC XPO1 degrader-1 Degrader
    PROTAC XPO1 degrader-1 (Compound 2c) 是一种 XPO1 降解剂。PROTAC XPO1 degrader-1 具有抗细胞增殖作用,还能诱导细胞凋亡 (Apoptosis),抑制 NF-κB 活性,并导致细胞周期阻滞于 G1 期。PROTAC XPO1 degrader-1 可以用于血液系统恶性肿瘤的研究 (粉色: 靶蛋白配体 (HY-170672); 黑色: Linker (HY-W010525); 蓝色: E3 连接酶配体 (HY-170671); E3 连接酶配体-Linker 偶联物 (HY-170673))。
    PROTAC XPO1 degrader-1
  • HY-163902
    SP100030 analogue 1 Inhibitor
    SP100030 analogue 1 (compound 11) 是一种 SP100030 (HY-110177) 类似物,一种选择性转录激活 (SITA) 抑制剂,基于 Jurkat 的 IL2-Luc 报告检测可以抑制 XPO1 依赖的 IL2 上调,EC50 为 137 nM。
    SP100030 analogue 1
  • HY-17536R
    Selinexor (Standard) Inhibitor
    Selinexor (Standard)是 Selinexor 的分析标准品。本产品用于研究及分析应用。Selinexor (KPT-330),是 KPT-185 的类似物。Selinexor 是一种口服有效的、选择性的 CRM1 抑制剂。
    Selinexor (Standard)
  • HY-157136
    LFS-1107
    LFS-1107 是一种可逆的 CRM1 抑制剂 (Kd: 12.5 pM)。LFS-1107 可选择性清除 ENKTL 细胞并用于肿瘤研究。
    LFS-1107
目录号 产品名 / 同用名 应用 反应物种