ζ-Stat (Synonyms: NSC37044)
目录号: PL09890 纯度: ≥95.0%
CAS No. :3316-02-7
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中文名称
ζ-Stat
中文别名
8-羟基-1,3,6-萘三磺酸
英文名称
ζ-Stat
英文别名
1,3,6-Naphthalenetrisulfonicacid, 8-hydroxy-;1-Naphthol, 3,6,8-trisulfo-;1-Naphthol,6,8-trisulfo-;1-naphthol-3,6,8-trisulfonic acid;1-naphthol-3,6,8-trisulphonic acid;1-Naphthylamin-3,6,8-trisulfonsaeure;8-hydroxy-naphthalene-1,3,6-trisulfonic acid;8-Hydroxy-naphthalin-1,3,6-trisulfonsaeure;AC1L2RRF;AC1Q6WID;CBDivE_016138;CHEMBL453929;CTK1C3734;Naphthol-(1)-trisulfonsaeure-(3.6.8);NSC37044;1-Naphthol-3,6,8-trisulfonicacid (6CI);1-Hydroxy-3,6,8-naphthalenetrisulfonic acid;3,6,8-Trisulfo-1-naphthol;8-Hydroxy-1,3,6-naphthalenetrisulfonic acid;ζ-Stat
Cas No.
3316-02-7
分子式
C10H8O10S3
分子量
384.36
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
ζ-Stat (NSC37044) 是一种特异且非典型的 PKC-ζ 的抑制剂,IC50 值为 5 μM。ζ-Stat 可以减少黑色素瘤细胞系的增殖并诱导细胞凋亡,在体外具有抗肿瘤活性。
生物活性
ζ-Stat (NSC37044) is a specific and atypical PKC-ζ inhibitor, with an IC 50 of 5 μM. ζ-Stat can reduce melanoma cell lines proliferation and induce apoptosis, and has antitumor activity in vitro.
性状
Solid
IC50 & Target[1][2]
aPKC-ζ 5 μM (IC50)
体外研究(In Vitro)
ζ-Stat (0.1-20 μM) shows only 13% inhibition on PKC-ι at 20 μM, but shows a significant inhibition on PKC-ζ as 51% at 5 μM level.
ζ-Stat (0.1-10 μM; 3 d) significantly decreases cell proliferation of SK-MEL-2 and MeWo upon increasing the concentrations.
ζ-Stat (7 or 10 μM; 24-72?h) and 5-FU in combination is able to decrease the viability of LoVo CRC cells by more than 75%.
ζ-Stat (5 μM; 3 d) shows a significant diminution of phosphorylated, total PKC-ζ, Bcl-2 and PARP levels, and increases Caspase-3 and cleaved-PARP levels in SK-MEL-2 and MeWo cells.
ζ-Stat (5 μM; 1-10 h) does not show significant cytotoxicity on MEL-F-NEO, SK-MEL-2 and MeWo 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]. Ratnayake WS, et, al. Oncogenic PKC-ι activates Vimentin during epithelial-mesenchymal transition in melanoma; a study based on PKC-ι and PKC-ζ specific inhibitors. Cell Adh Migr. 2018; 12(5):447-463.
[2]. Islam SMA, et, al. Atypical Protein Kinase-C inhibitors exhibit a synergistic effect in facilitating DNA damaging effect of 5-fluorouracil in colorectal cancer cells. Biomed Pharmacother. 2020 Jan; 121:109665.
溶解度数据
In Vitro: H2O : 62.5 mg/mL (162.61 mM; Need ultrasonic)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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