CK-636 (Synonyms: CK-0944636)
目录号: PL04559 纯度: ≥98%
CAS No. :442632-72-6
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中文名称
CK-636
中文别名
CK636 抑制剂;N-[2-(2-甲基-1H-吲哚-3-基)乙基]-2-噻吩甲酰胺
英文名称
CK-636
英文别名
CK-636;CK 636;N-[2-[(9aS)-1,3,4,9a-tetrahydropyrido[3,4-b]indol-2-yl]ethyl]thiophene-2-carboxamide;CK0944636;CK-0944636;N-[2-(2-Methyl-1H-indol-3-yl)ethyl]-2-thiophenecarboxamide;N-[2-(2-methyl-1H-indol-3-yl)ethyl]thiophene-2-carboxamide;N-[2-(2-methylindol-3-yl)ethyl]-2-thienylcarboxamide;N-(2-(2-methyl-1H-indol-3-yl)ethyl)thiophene-2-carboxamide;3dxk;ZERO/003249;Oprea1_603109;AOB6801;CK636;HMS3653J09;BCP09080;2325AH;SB19452;DB08235;ST038703;AK174334;BC600642
Cas No.
442632-72-6
分子式
C16H16N2Os
分子量
284.38
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
CK-636是具有细胞渗透性的Arp2/3 复合体抑制剂,能抑制肌动蛋白的聚合,对人,裂殖酵母和牛的 IC50 值分别为4 μM,24 μM和32 μM。CK636 抑制细胞迁移。
生物活性
CK-636 is a cell permeable inhibitor of Arp2/3 complex, that could inhibit actin polymerization, with IC 50 values of 4 μM, 24 μM and 32 μM for human, fission yeast and bovine, respectively. CK636 blocks cell migration.
性状
Solid
IC50 & Target[1][2]
IC50: 4/24/32 μM (Human/fission yeast/bovine Arp2/3).
体外研究(In Vitro)
CK-636 binds between Arp2 and Arp3, where it appears to block movement of Arp2 and Arp3 into their active conformation. CK-636 inserts into the hydrophobic core of Arp3 and alters its conformation. CK-636 prevents actin polymerization and the formation of actin filament comet tails by Listeria in infected SKOV3 cells (IC50=22 μM). Additionally, CK-636-treated T cells exhibits elongated morphology with sharp pseudopodia at the leading edges, while the breadth of the CK-636-treated T cells is about 30% less than that of DMSO-treated T cells. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Nolen BJ, et al. Characterization of two classes of small molecule inhibitors of Arp2/3 complex. Nature. 2009 Aug 20;460(7258):1031-4.
[2]. Kwon KW, et al. Migration of T cells on surfaces containing complex nanotopography. PLoS One. 2013 Sep 12;8(9):e73960.
[3]. Liang Ma, et al. Discovery of the migrasome, an
溶解度数据
In Vitro: DMSO : ≥ 49 mg/mL (172.30 mM)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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