12
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9063 |
Clathrin-IN-1
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Clathrin-IN-1 是一种网格蛋白抑制剂,可通过与网格蛋白的末端域相关联来抑制网格蛋白介导的内吞作用,有潜力用于抗癌的研究。 | |||
T25257 |
Clathrin-IN-25
Clathrin IN 25 |
||
Clathrin-IN-25 is the most effective clathrin terminal domain-amphiphysin inhibitor reported to date. | |||
T25256 |
Pitstop1
Clathrin inhibitor 1,Clathrin-inhibitor-1,Clathrin IN 1 |
||
Clathrin-IN-1 is a selective clathrin inhibitor that acts by addressing clathrin function in cell physiology with potential applications as an inhibitor of virus and pathogen entry and as a modulator of cell signaling. | |||
T72894 |
Clathrin-IN-2
|
||
Clathrin-IN-2 是网格蛋白介导的内吞作用(CME)的有效抑制剂,IC50值为 2.3 μM。 Clathrin-IN-2 还对dyn I GTPase 具有抑制作用,IC50值为 7.7 μM。 | |||
T26357 |
Pitstop 2
|
Apoptosis | Apoptosis |
Pitstop2 是一种选择性的两性蛋白结合的网格蛋白末端结构域抑制剂,IC50 值为 12 μM。 Pitstop2 严重干扰受体介导的内吞作用、HIV 进入和突触小泡循环。 | |||
T6822 |
Hydroxy-Dynasore
Dyngo-4a |
Dynamin | Cytoskeletal Signaling |
Hydroxy-Dynasore (Dyngo-4a) 是 Dynasore 结构模拟类似物,是一种改进的,低细胞毒性的 dynamin 通用抑制剂,抑制 dynamin 依赖性转铁蛋白的内吞作用的 IC50为 5.7 μM,对大脑重组 dynamin I 和重组鼠 dynamin II 的 IC50值分别为 0.38 μM 和 2.3μM。 | |||
T64369 |
Dynamin IN-2
|
Dynamin | Cytoskeletal Signaling |
Dynamin IN-2是一种Wiskostatin 类似物。Dynamin IN-2有效抑制 dynamin ,对 dynamin I GTPase 的 IC50 为 1.0 μM。Dynamin IN-2 可阻断网格蛋白介导的内吞作用 (CME),IC50 为 9.5 μM。 | |||
T64368 |
ES9-17
|
Others | Others |
ES9-17 是网格蛋白介导的内吞作用 (CME)的抑制剂。 CME 是植物胞外环境中质膜蛋白和分子内化的主要途径。ES9-17 抑制FM4-64和转铁蛋白的摄取。ES9-17 可以抑制拟南芥 (Arabidopsis) 幼苗的根生长。 | |||
T39050 |
Pitnot-2
|
||
Pitnot-2 is an inert analogue of the clathrin inhibitor Pitstop 2, commonly employed as a negative control in experimental studies. | |||
T61488 |
Dynole 2-24
|
||
Dynole 2 24 是一种基于吲哚的dynamin GTPase 抑制剂 (对 dynamin I 的IC50=0.56 μM)。Dynole 2 24 无毒,在体外和细胞内显示出增强的抗动力蛋白I 和II 的效力 (IC (CME)=1.9 μM)。Dynole 2 24 对 dynamin I 的选择性为4.4倍。Dynole 2 24在网格蛋白介导的内吞作用的细胞抑制剂中具有活性。CME: Clathrin mediated endocytosis | |||
T83891 |
Sulfonadyn-47
|
||
Sulfonadyn-47是一种dynamin抑制剂,能在无细胞测定中抑制dynamin的GTP酶活性(IC50 = 3.5 µM)。在U2OS细胞中,Sulfonadyn-47抑制clathrin介导的内吞作用(IC50 = 27.3 µM),同时在分离的大鼠脑突触体中抑制由去极化刺激的FM4-64摄取,后者是突触小泡内吞(SVE)的标志(IC50 = 12.3 µM)。在体内,Sulfonadyn-47(30和60 mg/kg)在6 Hz角膜电引发小鼠癫痫模型中具有抗惊厥活性。 | |||
T36368 |
2H-Cho-Arg (trifluoroacetate salt)
|
||
2H-Cho-Arg is a steroid-based cationic lipid that contains a 2H-cholesterol skeleton coupled to an L-arginine head group and can be used to facilitate gene transfection. It forms a complex with plasmid DNA (pDNA) and decreases pDNA migration in an electrophoretic mobility shift assay at +/- charge ratios of 4 or higher. 2H-Cho-Arg facilitates transfection of a luciferase gene into H1299 cells, an effect that is reversed by the lipid raft-mediated endocytosis inhibitor methyl-β-cyclodextrin and t... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15556 |
Ikarugamycin
|
Others | Others |
Ikarugamycin, an antibiotic, is an inhibitor of clathrin-mediated endocytosis (CME). |