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EB-3D

EB-3D

中文名稱EB-3D
中文同義詞1,1'-(((乙烷-1,2-二基雙(氧基))雙(4,1-亞苯基))雙(亞甲基))雙(4-(二甲氨基)吡啶-1-鎓)溴化物;化合物EB-3D;化合物EB-3D,10 MM DMSO 溶液;EB-3D 試劑;EB-3D 試劑
英文名稱EB-3D
英文同義詞EB-3D;ChoK inhibitor EB-3D;1,1'-(((Ethane-1,2-diylbis(oxy))bis(4,1-phenylene))bis(methylene))bis(4-(dimethylamino)pyridin-1-ium) bromide;lipid,inhibit,lymphoblastic,AMP-activated protein kinase,EB3D,acute,tumorigenesis,Apoptosis,homeostasis,dephosphorylation,AMPK,Inhibitor,EB 3D,leukemia,EB-3D,HepG2;EB-3D, 10 mM in DMSO
CAS號1839150-63-8
分子式C30H36BrN4O2+
分子量564.55
EINECS號
相關類別
Mol文件1839150-63-8.mol
結構式EB-3D 結構式

EB-3D 性質

儲存條件Inert atmosphere,Room Temperature
溶解度二甲基亞砜:50 mg/mL(77.59 mM)
形態(tài)固體
顏色白色至米白色

EB-3D 用途與合成方法

EB-3D 是一種有效的 choline kinase α (ChoKα) 的選擇性抑制劑,對ChoKα1的IC50值為1 μM。EB-3D 可在白血病T細胞中誘導 AMPK-mTOR 通路失調和凋亡。
TargetValue
ChoKα1
(Cell-free assay)
1 μM

EB-3D displays (0-100 μM; 72 hours) excellent antiproliferative activity against a wide cohort of T-leukemic cell lines, with GI GI 50 s 13 values in the nanomolar range.
EB-3D (1.25-5μM; 24 hours) induced apoptosis in leukemia cell lines.
EB-3D (0.5-1 μM; 24 hours) induces a G0/G1 arrest that lead to apoptosis.
EB-3D (0.3 μM; 48 hours) shows a first spike of activation of AMPKα after 30 minutes and a later increase in the phosphorylation of T172.
EB-3D (1-40 μM; 48?hours) inhibits cell growth in HepG2 cells with a GI 50 of 14.55 μM.
EB-3D induces deregulation of the AMPK-mTOR pathway and apoptosis in leukemia T-cells.

Cell Proliferation Assay

Cell Line: JURKAT, CCRF-CEM, HSB-2, MOLT-16, DNA-41, LOUCY, PEER, ALL-SIL cells
Concentration: 0.001, 0.01, 0.1, 1, 10, 100 μM
Incubation Time: 72 hours
Result: Inhibited JURKAT, CCRF-CEM, HSB-2, MOLT-16, DNA-41, LOUCY, PEER, and ALL-SIL cells growth with GI 50 s of 136.2, 478.8, 17.7, 0.9, 60.6, 200, 265, and 132 nM, respectively.

Apoptosis Analysis

Cell Line: Jurkat, CCRF-CEM and HSB-2 cells
Concentration: 1.25, 2.5, 5 μM
Incubation Time: 24 hours
Result: Induced apoptosis in leukemia cell lines.

Cell Cycle Analysis

Cell Line: Jurkat, CCRF-CEM and HSB-2 cells
Concentration: 0.5, 1 μM
Incubation Time: 24 hours
Result: Induces cell cycle arrest in G0/G1 phase.

Western Blot Analysis

Cell Line: Jurkat cells
Concentration: 0.3 μM
Incubation Time: 48 hours
Result: Showed a first spike of activation of AMPKα after 30 minutes of treatment and a later increase in the phosphorylation of T172. The increase in S79 phosphorylation of its main target ACC (acetyl-coenzyme A (CoA) carboxylase), followed the same pattern. This rapid activation of AMPK, in turn induced a consequent reduction in mTOR phosphorylation that is visible already at 30’ and that becomes amplified at longer time probably due to the interruption of feedback loops that are characteristic of mTOR connecting pathways.

EB-3D (1 mg/kg; i.p.; every other day) impairs mammary tumor growth in syngeneic orthotopic E0771-C57BL/6 mouse model.
EB-3D (2.5 mg/kg; every other day for 4 weeks) shows a reduction of the number of spontaneous lung macro- and micrometastasis.

Animal Model: E0771-C57BL/6 mice
Dosage: I.p.; every other day for 4 weeks
Administration: 2.5 mg/kg
Result: A reduction of the number of spontaneous lung macro- and micrometastasis.

安全信息

MSDS信息

更新日期產品編號產品名稱CAS號包裝價格
2026/06/05HY-115463EB-3D
EB-3D
1839150-63-85mg1900元
2026/06/05HY-115463EB-3D
EB-3D
1839150-63-810mM * 1mLin DMSO2694元

EB-3D 上下游產品信息

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