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204205-90-3

中文名稱 2-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
英文名稱 2-(1-(4-Chlorophenylmethyl)-1H-indol-3-yl)-2-oxo-N-(pyridin-4-yl)acetamide
CAS 204205-90-3
分子式 C22H16ClN3O2
分子量 389.83
MOL 文件 204205-90-3.mol
更新日期 2024/12/23 17:38:58
204205-90-3 結(jié)構(gòu)式 204205-90-3 結(jié)構(gòu)式

基本信息

中文別名
2-溴-2-(2-氟苯基)-1-環(huán)丙乙酮
2-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
英文別名
ZIO 301
Indibulin
Nascapine
lindiblin
2-[1-(4-Chlorobenzyl)-1H-indol-3-yl]-2-oxo-N-pyridin-4-ylacetamide
1H-Indole-3-acetamide, 1-[(4-chlorophenyl)methyl]-α-oxo-N-4-pyridinyl-
2-[1-[(4-chlorophenyl)methyl]indol-3-yl]-2-oxo-N-pyridin-4-ylacetamide
2-(1-(4-Chlorophenylmethyl)-1H-indol-3-yl)-2-oxo-N-(pyridin-4-yl)acetamide
2-(1-(4-Chlorophenylmethyl)-1H-indol-3-yl)-2-oxo-N-(pyridin-4-yl)acetamide ISO 9001:2015 REACH
所屬類別
醫(yī)藥中間體:芐基吡啶

物理化學(xué)性質(zhì)

密度1.31±0.1 g/cm3(Predicted)
儲存條件Sealed in dry,Store in freezer, under -20°C
溶解度DMSO:33.25(Max Conc. mg/mL);85.29(Max Conc. mM)
酸度系數(shù)(pKa)9.38±0.70(Predicted)
形態(tài)固體
顏色Off-white to yellow
2-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08HY-136492-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
Indibulin
204205-90-35mg700元
2024/11/08HY-136492-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
Indibulin
204205-90-310mM * 1mLin DMSO770元
2024/11/08HY-136492-(1-(4-氯芐基)-1H-吲哚-3-基)-2-氧代-N-(吡啶-4-基)乙酰胺
Indibulin
204205-90-310mg1120元

常見問題列表

生物活性
Indibulin (ZIO 301, D 24851, Zybulin) 是一種口服的 tubulin assembly 抑制劑,并具有有效的抗癌活性。Indibulin 可誘導(dǎo)有絲分裂的停滯和凋亡。
靶點(diǎn)
TargetValue
Tubulin
()
體外研究

Indibulin (300-2100 nM; 48?hours) inhibits the proliferation of MCF-7 cells with an IC50 of 150?nM.
Indibulin (300, 600 nM; 48?hours) blockes the cells in the G2/M phase indicating that indibulin blockes the progression of the cell cycle at mitosis.
Indibulin (150-600 nM; 24?hours) induces apoptosis in MCF-7 cells.
Indibulin (150-600 nM; 48?hours) with 300 and 600?nM generates cleaved fragments of PARP protein the treatment of MCF-7 cells.

Cell Proliferation Assay

Cell Line: MCF-7 cells
Concentration: 300, 600, 900, 1200, 1500, 1800, 2100 nM
Incubation Time: 48?hours
Result: Inhibited the proliferation of MCF-7 cells with an IC 50 of 150?nM.

Cell Cycle Analysis

Cell Line: MCF-7 cells
Concentration: 300, 600 nM
Incubation Time: 48?hours
Result: Blocked the cells in the G2/M phase of the cell cycle.

Apoptosis Analysis

Cell Line: MCF-7 cells
Concentration: 150, 300 and 600?nM
Incubation Time: 24?hours
Result: Induced apoptosis in MCF-7 cells.

Western Blot Analysis

Cell Line: MCF-7 cells
Concentration: 150, 300 and 600?nM
Incubation Time: 48?hours
Result: Generated cleaved fragments of PARP protein in 300 and 600?nM.
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