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ZINC05007751
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
ZINC05007751图片
CAS NO:591239-68-8
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议

产品介绍
ZINC05007751 是一种有效的 NIMA 相关激酶NEK6抑制剂,IC50为 3.4 μM。ZINC05007751 对一组人类癌细胞系显示出抗增殖活性,并且在 BRCA2 突变的卵巢癌细胞系中显示出与顺铂和紫杉醇的协同效应。ZINC05007751 对 NEK1 和 NEK6 具有很强的选择性,但对 NEK2、NEK7 和 NEK9 没有明显的活性。
生物活性

ZINC05007751 is a potent NIMA-related kinaseNEK6inhibitor with anIC50of 3.4 μM. ZINC05007751 shows antiproliferative activity against a panel of humancancercell lines, and displays a synergistic effect with Cisplatin and Paclitaxel in a BRCA2 mutated ovariancancercell line. ZINC05007751 is very selective against NEK1 and NEK6 with no significant activity was observed against NEK2,NEK7, and NEK9[1].

体外研究
(In Vitro)

ZINC05007751 (6 μM-190 μM; 24 hours) inhibits the growth of MDA-MB-231, PEO1, NCI-H1299 and HCT-15 with IC50 below 100 μM[1].
ZINC05007751 induces perturbation of PEO1 cell cycle[1].
ZINC05007751 (ovarian cancer cells PEO1) shows synergism with Cisplatin, resulting in a significant reduction of Cisplatin IC50 from 7.9 to 0.1 μM, with combination ZINC05007751 (44 μM) + Cisplatin (10 μM) exhibiting the greatest synergistic effect[1].

Cell Cytotoxicity Assay[1]

Cell Line:MDA-MB-231, PEO1, NCI-H1299 and HCT-15 cells
Concentration:6 μM-190 μM
Incubation Time:24 hours
Result:Inhibited the growth of MDA-MB-231, PEO1, NCI-H1299 and HCT-15.
分子量

304.30

性状

Solid

Formula

C18H12N2O3

CAS 号

591239-68-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

溶解性数据
In Vitro: 

DMSO : 8.33 mg/mL(27.37 mM;ultrasonic and warming and heat to 60℃)

配制储备液
浓度溶剂体积质量1 mg5 mg10 mg
1 mM3.2862 mL16.4312 mL32.8623 mL
5 mM0.6572 mL3.2862 mL6.5725 mL
10 mM0.3286 mL1.6431 mL3.2862 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month (protect from light)。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。