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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T60416 | CRM1 degrader 1 | ||
CRM1 degrader 1 (1l) 是一种低毒的CRM1降解剂,可诱导胃癌细胞凋亡并选择性抑制胃癌细胞的增殖。 | |||
T79654 |
CRM1-IN-1
|
CRM1 | Membrane transporter/Ion channel |
CRM1-IN-1 (Compound KL1) 为非共价CRM1抑制剂,能诱导核CRM1降解(IC50: 0.27 μM),抑制CRM1介导的核输出与细胞增殖,同时触发结直肠癌细胞凋亡 (apoptosis)。 | |||
T79655 |
CRM1-IN-2
|
CRM1 | Membrane transporter/Ion channel |
CRM1-IN-2(Compound KL2)为非共价CRM1抑制剂,能够定位CRM1于核外围,耗尽核内CRM1,从而抑制CRM1介导的核输出。该化合物能抑制结直肠癌细胞的生长并诱导细胞凋亡(apoptosis)。 | |||
T24269 |
KPT-251
KPT251 |
Others | Others |
KPT-251 是一种选择性核输出抑制剂。 | |||
T15735 |
Leptomycin B
CI 940,LMB,来普霉素B |
CRM1; Antibiotic; Antifungal | Membrane transporter/Ion channel; Microbiology/Virology |
Leptomycin B (LMB) 是一种抗真菌抗生素,可阻断真核细胞周期,抑制蛋白出核转运。Leptomycin 通过半胱氨酸残基处的共价修饰使 CRM1/exportin 1失活。它 | |||
T2425 |
KPT185
KPT-185,KPT 185 |
CRM1 | Membrane transporter/Ion channel |
KPT185 (KPT 185) 是一种选择性 CRM1 抑制剂,可诱导细胞凋亡、细胞周期停滞。 | |||
T6074 |
KPT276
KPT-276,KPT 276 |
CRM1 | Membrane transporter/Ion channel |
KPT276 (KPT 276) 是一种口服生物可利用的核输出选择性抑制剂(SINE),不可逆地与 CRM1 结合并阻断 CRM1 的功能。 | |||
T14885 |
CBS9106
SL-801 |
CRM1 | Membrane transporter/Ion channel |
CBS9106 (SL-801) is a reversible oral inhibitor of CRM1 with CRM1 degrading and antitumor activities. CBS9106 arrests the cell cycle and inducing apoptosis in a time- and dose-dependent manner for a broad spectrum of cancer cells. | |||
T6123 |
Verdinexor
KPT-335 |
CRM1 | Membrane transporter/Ion channel |
Verdinexor (KPT-335) 是一种特异性 XPO1/CRM1 抑制剂,具有口服生物利用度。 | |||
T1844 |
KPT330,(E)-
(E)-RN,KPT-330,KPT330,KPT 330 |
Others; CRM1 | Membrane transporter/Ion channel; Others |
(E)-RN (KPT 330) 是一种 CRM1 选择性核输出抑制剂。它抑制细胞核中的蛋白质运输并诱导间皮瘤细胞中的细胞周期停滞和凋亡。 | |||
T6106 |
Selinexor (KPT-330)
Selinexor,KPT-330,塞利尼索 |
CRM1 | Membrane transporter/Ion channel |
Selinexor (KPT-330) 是一种 CRM1 的小分子抑制剂,具有选择性和口服活性。Selinexor 可以阻滞细胞周期、诱导细胞凋亡,具有抗肿瘤活性,可以用于治疗多发性骨髓瘤。 | |||
T16548 | PKF050-638 | HIV Protease | Microbiology/Virology; Proteases/Proteasome |
PKF050-638 inhibits the CRM1-mediated Rev nuclear export by disrupting CRM1-NES interaction. PKF050-638 is an effective and selective inhibitor of HIV-1 Rev (IC50=0.04 μM). | |||
T11766 |
Eltanexor Z-isomer
KPT-8602 (Z-isomer) |
Others | Others |
Eltanexor Z-isomer exhibits different inhibitory effects on Z138, MM15, 3T3 cell lines, with IC50s of 100 nM-50 μM, < 100 nM, > 30 μM, respectively.Eltanexor Z-isomer is the less active isomer of KPT-8602. KPT-8602 is a potent CRM1 inhibitor. | |||
T81936 |
LFS-1107
|
CRM1 | Membrane transporter/Ion channel |
LFS-1107为一种CRM1抑制剂,具有可逆特性(Kd: 12.5 pM)。该化合物能够选择性地清除ENKTL细胞,常用于肿瘤学研究。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T11837 |
Leptomycin A
|
CRM1 | Membrane transporter/Ion channel |
Leptomycin A, a metabolite derived from Streptomyces, acts as an inhibitor of CRM1 (exportin 1) and effectively suppresses HIV-1 replication. Compared to Leptomycin B, it exhibits lesser potency. Leptomycin A hampers the interaction between CRM1 and nuclear export signals, effectively hindering the nuclear export of a wide array of proteins. |