KS106
目录号: PL04171 纯度: ≥99%
CAS No. :2408477-50-7
商品编号 规格 价格 会员价 是否有货 数量
PL04171-5mg 5mg ¥3709.09 请登录
PL04171-10mg 10mg ¥5934.55 请登录
PL04171-25mg 25mg ¥11745.45 请登录
PL04171-50mg 50mg ¥17927.27 请登录
PL04171-100mg 100mg 询价 询价
PL04171-200mg 200mg 询价 询价
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
中文名称
KS106
英文名称
KS106
英文别名
Carbamimidothioic acid, [4-​[[2,​3-​dihydro-​2,​3-​dioxo-​5-​(trifluoromethyl)​-​1H-​indol-​1-​yl]​methyl]​phenyl]​methyl ester, hydrobromide (1:1);KS106
Cas No.
2408477-50-7
分子式
C18H15BrF3N3O2S
分子量
474.29
包装储存
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
产品详情
KS106 是一种有效的 ALDH 抑制剂,对 ALDH1A1、ALDH2 和 ALDH3A1 的 IC50 分别为 334、2137、360 nM。KS106 具有低毒性的抗增殖和抗癌作用。KS106 显著增加 ROS 活性、脂质过氧化和有毒醛的积累。KS106 诱导细胞凋亡 (apoptosis) 和细胞周期停滞在 G2/M 期。
生物活性
KS106 is a potent ALDH inhibitor with IC 50 s of 334, 2137, 360 nM for ALDH1A1, ALDH2, and ALDH3A1, respectively. KS106 shows antiproliferative and anticancer effects with low low toxic.KS106 significantly increases ROS activity, lipid peroxidation and toxic aldehyde accumulation. KS106 induces apoptosis and cell cycle arrest at the G2/M phase.
性状
Solid
IC50 & Target[1][2]
ALDH1 ALDH2
体外研究(In Vitro)
KS106 (compound 3h) (0-100 μM; 72 h) shows anti-proliferative activity with IC50s of 5.7, 5.7, 5.7, 4.9, 1.5, 2.6, 1.6, 1.7, 2.2, 20.7 μM for UACC 903, 1205 Lu, HCT116, HT29, NCIH929, U266, RPMI8226, MM.1R, MM.1S, FF2441 cells, respectively.
KS106 (5 μM, 24 h) induces apoptosis and cell cycle arrest at the G2/M phase. has not independently confirmed the accuracy of these methods. They are for reference only.Apoptosis Analysis
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moisture and light In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
参考文献
[1]. Dinavahi SS, et al. Design, synthesis characterization and biological evaluation of novel multi-isoform ALDH inhibitors as potential anticancer agents. Eur J Med Chem. 2020 Feb 1;187:111962.
溶解度数据
In Vitro: DMSO : 100 mg/mL (210.84 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

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。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2