166977-43-1
中文名称
BMS453
英文名称
BMS453
CAS
166977-43-1
分子式
C27H24O2
分子量
380.48
MOL 文件
166977-43-1.mol
更新日期
2024/07/23 09:31:05
166977-43-1 结构式
基本信息
中文别名
化合物BMS 453 英文别名
BMS453BMS-189453 (BMS189453
(E)-4-[2-(5,5-Dimethyl-8-phenyl-5,6-dihydronaphthalen-2-yl)vinyl]benzoic acid
(E)-4-[2-(5,6-Dihydro-5,5-dimethyl-8-phenyl-2-naphthalenyl)ethenyl]-benzoic acid
4-[(1E)-2-(5,6-Dihydro-5,5-dimethyl-8-phenyl-2-naphthalenyl)ethenyl]-benzoicacid
Benzoic acid, 4-[(1E)-2-(5,6-dihydro-5,5-dimethyl-8-phenyl-2-naphthalenyl)ethenyl]-
物理化学性质
沸点560.9±50.0 °C(Predicted)
密度1.167±0.06 g/cm3(Predicted)
储存条件-20°C储存
溶解度DMSO：可溶10mg/mL，澄清
酸度系数(pKa)4.27±0.10(Predicted)
形态粉末
颜色白色至米色
BMS453价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2025/02/08 | HY-100608 | BMS453 | 166977-43-1 | 1 mg | 359元 |
| 2025/02/08 | HY-100608 | BMS453 BMS453 | 166977-43-1 | 10 mM * 1 mLin DMSO | 710元 |
| 2025/02/08 | HY-100608 | BMS453 BMS453 | 166977-43-1 | 5mg | 848元 |
常见问题列表
生物活性
BMS453 (BMS-189453) 是一种合成类维生素 A，是一种 RARβ 激动剂和 RARα/RARγ 拮抗剂。BMS453 主要通过诱导活性 TGFβ 来抑制乳腺细胞生长。体外研究
BMS453 (1 μM; 11 hours; 184 and HMEC cells) treatment inhibits the proliferation of normal breast cell growth without significantly inducing apoptosis.
BMS453 (1 μM; 5 days; 184 and HMEC cells) treatment inhibits normal breast cell proliferation by causing G1 arrest.
BMS453 (1 μM; 24-72 hours; 184 cells) treatment induces Rb hypophosphorylation and decrease CDK2 kinase activity. BMS453 increases total p21 protein levels and CDK2-bound p21 protein, but does not change CDK4-bound p21.
BMS453 inhibits breast cell growth predominantly through the induction of active TGFβ.
Cell Proliferation Assay
| Cell Line: | Normal human mammary epithelial cells (184 and HMEC) |
| Concentration: | 1 μM |
| Incubation Time: | 11 hours |
| Result: | Inhibited 3 H-thymidine uptake in normal breast cells (184 and HMEC) by 40 %. |
Cell Cycle Analysis
| Cell Line: | Normal human mammary epithelial cells (184 and HMEC) |
| Concentration: | 1 μM |
| Incubation Time: | 5 days |
| Result: | Increased the proportion of cells in G0/G1 phase and decreased the proportion of cells in S phase. |
Western Blot Analysis
| Cell Line: | 184 cells |
| Concentration: | 1 μM |
| Incubation Time: | 24 hours, 48 hours, 72 hours |
| Result: | Induced Rb hypophosphorylation and decrease CDK2 kinase activity. |