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92953-10-1

中文名稱 氯非銨甲苯磺酸鹽
英文名稱 CLOFILIUM TOSYLATE
CAS 92953-10-1
分子式 C28H44ClNO3S
分子量 510.17
MOL 文件 92953-10-1.mol
更新日期 2024/06/03 14:41:41
92953-10-1 結(jié)構(gòu)式 92953-10-1 結(jié)構(gòu)式

基本信息

中文別名
氯非銨甲苯磺酸鹽
英文別名
CLOFILIUM TOSYLATE
4-CHLORO-N,N-DIETHYL-N-HEPTYLBENZENEBUTANAMINIUM TOSYLATE
4-chloro-n,n-diethyl-n-heptyl-benzenebutanaminiusaltwith4-methylbenzenes
N-(4-(4-CHLOROPHENYL)BUTYL)-N,N-DIETHYLHEPTAN-1-AMINIUM 4-METHYLBENZENESULFONATE
所屬類別
化學(xué)試劑:有機(jī)試劑

物理化學(xué)性質(zhì)

儲(chǔ)存條件4°C, protect from light
溶解度H2O: soluble
形態(tài)solid
顏色white
水溶解性H2O: soluble

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)有害 (GHS07)
GHS07
警示詞警告
危險(xiǎn)性描述H302
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類別碼22
安全說明36
WGK Germany3
RTECS號(hào)CY9040870
氯非銨甲苯磺酸鹽價(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
2025/12/22HY-33350氯非銨甲苯磺酸鹽
Clofilium tosylate
92953-10-11 mg308元
2025/12/22HY-33350氯非銨甲苯磺酸鹽
Clofilium tosylate
92953-10-15 mg728元
2025/12/22HY-33350氯非銨甲苯磺酸鹽
Clofilium tosylate
92953-10-110mM * 1mLin DMSO864元

常見問題列表

生物活性
Clofilium tosylate 是一種鉀通道 (potassium channel) 阻滯劑,作用于人早幼粒細(xì)胞白血病 (HL-60) 細(xì)胞,激活 caspase-3 而誘導(dǎo)凋亡。具有抗心律失常作用。
靶點(diǎn)

Potassium channel

體外研究

HL-60 cells treated with Clofilium (0-20 μM; 24, 48, and 72 hours) lead to suppression of viability and proliferation in both time and concentration-dependent manners. Cell viability decreases significantly in HL-60 cells treated with 2.5 μM to 10 μM of Clofilium.
Clofilium (10 μM, 12 hours) induces the proteolytic cleavage of inactive procaspase-3, p34 into its active form, p17 and subsequent cleavage of its substrate PARP at 2 h after exposure to 10 mM Clofilium. However, there is no significant change in expression of Bcl-2 and Bax proteins.

Cell Viability Assay

Cell Line: HL-60 cells
Concentration: 0-20 μM
Incubation Time: 24, 48, and 72 hours
Result: Inhibited HL-60 cells with IC 50 s of 6.3 μM for 24 hours, 3.4 μM for 48 hours, 2.4 μM for 72 hours, respectively.

Western Blot Analysis

Cell Line: HL-60 cells
Concentration: 10 μM
Incubation Time: 12 hours
Result: Induced proteolytic cleavage of caspase-3 and subsequent cleavage of its substrate, PARP, while Bcl-2 and Bax proteins were unaltered.
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