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1309444-75-4

1309444-75-4

中文名稱1309444-75-4
中文同義詞化合物 T11739;化合物 K145
英文名稱K145
英文同義詞K145;3-(2-Aminoethyl)-5-[3-(4-butoxyphenyl)propylidene]-2,4-thiazolidinedione;2,4-Thiazolidinedione, 3-(2-aminoethyl)-5-[3-(4-butoxyphenyl)propylidene]-;K145 ,K145 HCl salt;K145,K-145
CAS號1309444-75-4
分子式C18H24N2O3S
分子量348.46
EINECS號
相關(guān)類別
Mol文件1309444-75-4.mol
結(jié)構(gòu)式1309444-75-4 結(jié)構(gòu)式

1309444-75-4 性質(zhì)

溶解度溶于二甲基亞砜
形態(tài)粉末

1309444-75-4 用途與合成方法

K145 是一種選擇性的,具有底物競爭性和口服活性的 SphK2 抑制劑,IC50 為 4.3 μM,Ki 為 6.4 μM。K145 對 SphK1 和其他蛋白激酶沒有活性。K145 可誘導(dǎo)細(xì)胞凋亡,并具有強大的抗腫瘤活性。

IC50: 4.3 μM (SphK2)
Ki: 6.4 μM (SphK2)

K145 (0-10 μM; 24-72 hours; U937 cells) treatment significantly inhibits the growth of U937 cells in a concentration-dependent manner.
K145 (10 μM; 24 hours; U937 cells) treatment significantly induces apoptosis in U937 cells.
K145 (4-8 μM; 3 hours; U937 cells) treatment decreases the phosphorylation of ERK and Akt.
Treatment with K145 (10 μM) causes a decrease of total cellular S1P without significant effects on ceramide levels.

Cell Viability Assay

Cell Line: U937 cells
Concentration: 0 μM, 4 μM, 6 μM, 8 μM, 10 μM
Incubation Time: 24 hours, 48 hours, 72 hours
Result: Significantly inhibited the growth of U937 cells in a concentration-dependent manner.

Apoptosis Analysis

Cell Line: U937 cells
Concentration: 10 μM
Incubation Time: 24 hours
Result: Significantly induced apoptosis in U937 cells.

Western Blot Analysis

Cell Line: U937 cells
Concentration: 4 μM, 8 μM
Incubation Time: 3 hours
Result: Phosphorylated ERK and Akt were decreased.

K145 (50 mg/kg; oral gavage; daily; for 15 days; BALB/c-nu mice) treatment significantly inhibits the growth of U937 tumors in nude mice.

Animal Model: BALB/c-nu mice injected with U937 cells
Dosage: 50 mg/kg
Administration: Oral gavage; daily; for 15 days
Result: Oral gavage; daily; for 15 daysInhibited the growth of U937 tumors at 50 mg/kg dose and no apparent toxicity was observed.

安全信息

MSDS信息

1309444-75-4 上下游產(chǎn)品信息

"1309444-75-4"相關(guān)產(chǎn)品信息
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