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203192-01-2

中文名稱 化合物MN58B
英文名稱 MN58b
CAS 203192-01-2
分子式 C32H40BrN4+
分子量 560.6
MOL 文件 203192-01-2.mol
更新日期 2025/05/09 09:36:20
203192-01-2 結(jié)構(gòu)式 203192-01-2 結(jié)構(gòu)式

基本信息

中文別名
化合物MN58B
英文別名
MN58b
1-[[4-[4-[4-[[4-(dimethylamino)pyridin-1-ium-1-yl]methyl]phenyl]butyl]phenyl]methyl]-N,N-dimethylpyridin-1-ium-4-amine

物理化學(xué)性質(zhì)

儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO:14.71(Max Conc. mg/mL);22.97(Max Conc. mM)
形態(tài)Solid
顏色White to off-white

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
防范說(shuō)明P280-P305+P351+P338
化合物MN58B價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2025/02/08HY-108431化合物MN58B
MN58b
203192-01-21mg3500元
2023/01/06S0998化合物MN58B
MN58b
203192-01-21mg6036.03元

常見(jiàn)問(wèn)題列表

生物活性
MN58b 是一種選擇性的 choline kinase α (CHKα) 抑制劑,可抑制磷酸膽堿的合成。MN58b 通過(guò)誘導(dǎo)凋亡來(lái)減少細(xì)胞生長(zhǎng),并具有抗腫瘤活性。
靶點(diǎn)

Choline kinase α (CHKα)

體外研究

The IC 50 s of MN58b for parental and Gemcitabine-resistant Suit2 007 cells are 3.14 μM and 0.77 μM, respectively.
MN58b (1-5 μM; 72 hours; SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells) has a marked effect on colony formation at 1 μM, and growth is completely abolished at 5 μM in all the cell lines.
MN58b ((1-10 μM; 24-48 hours; SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells) induces apoptosis and this response correlates with CHKα expression.

Cell Viability Assay

Cell Line: SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells
Concentration: 1 μM, 5 μM
Incubation Time: 72 hours
Result: Inhibited cells growth.

Apoptosis Analysis

Cell Line: SK-PC-1, Suit2 008, IMIM-PC2, and RWP-1 cells
Concentration: 1 μM, 2 μM, 5 μM, 10 μM
Incubation Time: 24 and 48 hours
Result: Induced cell apoptosis.
體內(nèi)研究

MN58b (4 mg/kg; intraperitoneal injection; once a day; for 5 days; MF-1 nude mice) treatment significantly decreases phosphomonoesters in both HT29 and MDA-MB-231 xenografts. Phosphocholine levels are found to correlate with choline kinase activities.

Animal Model: MF-1 nude mice with HT29 or MDA-MB-231 cells
Dosage: 4 mg/kg
Administration: Intraperitoneal injection; once a day; for 5 days
Result: Phosphomonoesters decreased significantly.
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