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123134-61-2

中文名称 1-(2-氨基苯基)-3-(3-硝基苯基)-2-丙烯-1-酮
英文名称 1-(2-Aminophenyl)-3-(3-nitrophenyl)-2-propen-1-one
CAS 123134-61-2
分子式 C15H12N2O3
分子量 268.27
MOL 文件 123134-61-2.mol
更新日期 2024/09/29 16:47:05
123134-61-2 结构式 123134-61-2 结构式

基本信息

中文别名
1-(2-氨基苯基)-3-(3-硝基苯基)-2-丙烯-1-酮
1-(2-氨基苯基)-3-(3-硝基苯基)丙-2-烯-1-酮
英文别名
BIA
TMBIM6 antagonist-1
β-(2,5-Dihydro-5-oxoisoxazole-2-yl)-L-alanine
2-Propen-1-one, 1-(2-aminophenyl)-3-(3-nitrophenyl)-
(2S)-3-[(2,5-Dihydro-5-oxoisoxazole)-2-yl]-2-aminopropanoic acid

物理化学性质

沸点482.1±45.0 °C(Predicted)
密度1.315±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度DMSO: 50 mg/mL (186.38 mM)
酸度系数(pKa)-0.47±0.10(Predicted)
形态Solid
颜色Light yellow to yellow

常见问题列表

生物活性
TMBIM6 antagonist-1 是一个有潜力的 TMBIM6 拮抗剂,抑制 TMBIM6 与 mTORC2 结合,降低 mTORC2 活性,调节TMBIM6 释放 Ca2+。
体外研究

TMBIM6 antagonist-1 (BIA, 0.5-10 μM, 3 days) significantly and dose-dependently inhibits cell viability in HT1080, MCF7, MDA-MB-2341 and SKBR3 cells, with IC 50 values of 1.7 ± 0.1 μM for HT1080, 2.6 ± 0.4 μM for MCF cells, 2.6 ± 0.5 μM for MDA-MB-231 cells, and 2.4 ± 0.4 μM for SKBR3 cells, respectively.
TMBIM6 antagonist-1 (BIA, 10 μM) treatment decreases cell migration in HT1080, MCF7, MDA-MB-231, and SKBR3 cells, not TMBIM6 KO HT1080 cells.

Cell Viability Assay

Cell Line: HT1080, MCF7, MDA-MB-2341 and SKBR3 cells.
Concentration: 0.5-10 μM.
Incubation Time: 3 days.
Result: Inhibited cell viability.

Western Blot Analysis

Cell Line: WT and TMBIM6 KO HT1080 cells.
Concentration: 0, 2, 5 μM.
Incubation Time:
Result: Downregulated the protein levels of AKT-pS473.
体内研究

TMBIM6 antagonist-1 (1 mg/kg, IP 5 days per week during 25 days) significantly impaires cell-driven tumor growth.

Animal Model: Six- to eight-week BklNbt:BALB/c/nu/nu old mice (HT1080 and MDA-MB-231 cells).
Dosage: 1 mg/kg.
Administration: IP 5 days per week during 25 days.
Result: Impaired cell-driven tumor growth.
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