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1875036-74-0

中文名稱 化合物 T14568
英文名稱 BI8622
CAS 1875036-74-0
分子式 C25H26N6O
分子量 426.51
MOL 文件 1875036-74-0.mol
1875036-74-0 結(jié)構(gòu)式 1875036-74-0 結(jié)構(gòu)式

基本信息

中文別名
化合物 T14568
英文別名
BI8622
BI8622 (BI-8622

物理化學(xué)性質(zhì)

沸點(diǎn)632.6±55.0 °C(Predicted)
密度1.29±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMSO : 125 mg/mL (293.08 mM; Need ultrasonic)
酸度系數(shù)(pKa)11.59±0.70(Predicted)
形態(tài)Solid
顏色White to off-white

常見問題列表

生物活性
BI8622 是一種泛素連接酶 HUWE1 特異性拮抗劑,IC50 為 3.1 μM。
靶點(diǎn)

IC50: 3.1 μM (HUWE1)

體外研究

BI8622 induces HUWE1 ectopically expresses to abolish ubiquitination of MCL1 with an IC 50 value of 6.8 μM in HeLa cells.
BI8622 suppresses colony formation of Ls174T cells with estimated IC 50 value of 8.4 μM.
BI8622 (10 μM; 1-4 days) treatment retards passage of Ls174T cells through all phases of the cell cycle, with the effect being strongest for G1.
BI8622 (0-50 μM; 16 hours) retards the degradation of MCL1 in response to UV irradiation by inhibiting HUWE1 in HeLa cells.
BI8622 inhibits MYC-dependent transactivation in colorectal cancer cells.

Cell Cycle Analysis

Cell Line: Ls174T cells
Concentration: 0 μM, 5 μM,10 μM, 15 μM, 20 μM
Incubation Time: 0-4 days
Result: Retarded passage of Ls174T cells through all phases of the cell cycle, with the effect being strongest for G1.

Western Blot Analysis

Cell Line: HeLa cells
Concentration: 0 μM, 10 μM, 20 μM
Incubation Time: 16 hours
Result: Retarded the degradation of MCL1 in response to UV irradiation by inhibiting HUWE1 in HeLa cells.
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