前往化源商城

KS106

更新时间:2025-08-25 22:59:40

KS106结构式
KS106结构式
品牌特惠专场
常用名 KS106 英文名 KS106
CAS号 2408477-50-7 分子量 474.29
密度 N/A 沸点 N/A
分子式 C18H15BrF3N3O2S 熔点 N/A
MSDS N/A 闪点 N/A

 KS106用途


KS106是一种有效的ALDH抑制剂,ALDH1A1、ALDH2和ALDH3A1的IC50分别为334、2137、360 nM。KS106具有低毒的抗增殖和抗癌作用。KS106显著增加活性氧活性、脂质过氧化和毒性醛的积累。KS106在G2/M期诱导细胞凋亡和细胞周期阻滞[1]。

 KS106名称

英文名 KS106

 KS106生物活性

描述 KS106是一种有效的ALDH抑制剂,ALDH1A1、ALDH2和ALDH3A1的IC50分别为334、2137、360 nM。KS106具有低毒的抗增殖和抗癌作用。KS106显著增加活性氧活性、脂质过氧化和毒性醛的积累。KS106在G2/M期诱导细胞凋亡和细胞周期阻滞[1]。
相关类别
靶点实验

IC50: 334 nM (ALDH1A1); 2137 nM (ALDH2); 360 nM (ALDH3A1)[1]

体外研究 KS106(化合物3h)(0-100µM;72 h)对UACC 903、1205 Lu、HCT116、HT29、NCIH929、U266、RPMI8226、MM的IC50为5.7、5.7、5.7、4.9、1.5、2.6、1.6、1.7、2.2、20.7µM,显示出抗增殖活性。1R,毫米。分别为1S、FF2441细胞[1]。KS106(5µM,24 h)在G2/M期诱导细胞凋亡和细胞周期阻滞[1]。凋亡分析【1】细胞系:HCT116、HT29细胞浓度:5µM孵育时间:24小时结果:诱导细胞凋亡。细胞周期分析【1】细胞系:HCT116细胞浓度:5µM孵育时间:24 h结果:诱导细胞周期阻滞于G2/M期。
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.

 KS106物理化学性质

分子式 C18H15BrF3N3O2S
分子量 474.29

 KS106靶点实验

查看更多实验

实验名称:Antiproliferative activity against human UACC 903 cells measured after 72 hrs by MTS ...
来源:ChEMBL
靶标:UACC-903
External Id:CHEMBL4708029
实验名称:Inhibition of ALDH3A1 (unknown origin) assessed as NADH formation using 4-nitrobenzal...
来源:ChEMBL
靶标:Aldehyde dehydrogenase, dimeric NADP-preferring
External Id:CHEMBL4708028
实验名称:Antiproliferative activity against human HCT116 cells measured after 72 hrs by MTS as...
来源:ChEMBL
靶标:HCT-116
External Id:CHEMBL4708031
实验名称:Antiproliferative activity against human 1205Lu cells measured after 72 hrs by MTS as...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4708030
实验名称:Antiproliferative activity against human NCIH929 cells measured after 72 hrs by MTS a...
来源:ChEMBL
靶标:NCI-H929
External Id:CHEMBL4708033
实验名称:Antiproliferative activity against human HT-29 cells measured after 72 hrs by MTS ass...
来源:ChEMBL
靶标:HT-29
External Id:CHEMBL4708032
实验名称:Antiproliferative activity against human RPMI8226 cells measured after 72 hrs by MTS ...
来源:ChEMBL
靶标:RPMI-8226
External Id:CHEMBL4708035
实验名称:Antiproliferative activity against human U266 cells measured after 72 hrs by MTS assa...
来源:ChEMBL
靶标:U-266
External Id:CHEMBL4708034
实验名称:Inhibition of ALDH2 (unknown origin) assessed as NADH formation using acetaldehyde as...
来源:ChEMBL
靶标:Aldehyde dehydrogenase, mitochondrial
External Id:CHEMBL4708027
实验名称:Inhibition of ALDH1A1 (unknown origin) assessed as NADH formation using propionaldehy...
来源:ChEMBL
靶标:Aldehyde dehydrogenase 1A1
External Id:CHEMBL4708026
共24条,当前第1页,共3页
1
2
3
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。