中文名称: BMS453
英文名称: BMS453
CAS No: 166977-43-1
分子式: C27H24O2
分子量: 380.48
B11377 BMS453 ≥98% (psaitong)
包装规格:
5mg in glass bottle
产品描述:

基本信息

产品编号:

B11377

产品名称:

BMS453

CAS:

166977-43-1

 

储存条件

粉末

-20℃

四年

 

 

分子式:

C27H24O2

溶于液体

-80℃

六个月

分子量

380.48

-20℃

一个月

化学名: 

(E)-4-[2-(5,6-Dihydro-5,5-dimethyl-8-phenyl-2-naphthalenyl)ethenyl]-benzoic acid

生物活性

产品描述

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。

靶点

 

体外研究

BMS453 (1μM; 11 hours; 184 and HMEC cells) treatment inhibits the proliferation of normal breast cell growth without significantly inducing apoptosis.

BMS453 (1μM; 5 days; 184 and HMEC cells) treatment inhibits normal breast cell proliferation by causing G1 arrest.

BMS453 (1μM; 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:

1μM

Incubation Time:

11 hours

Result:

Inhibited 3H-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:

1μM

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:

1μM

Incubation Time:

24 hours, 48 hours, 72 hours

Result:

Induced Rb hypophosphorylation and decrease CDK2 kinase activity.

保存条件:
-20℃
UN码:
HazardClass:
危害声明:
安全说明:
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本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系,公式为:
质量 (g) = 浓度 (mol/L) x 体积 (L) x 分子量 (g/mol)

摩尔浓度计算公式

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用本工具协助配置特定浓度的溶液,使用的计算公式为:
开始浓度 x 开始体积 = 最终浓度 x 最终体积

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    C2=C1/X C2: LOG(C2):
    C3=C2/X C3: LOG(C3):
    C4=C3/X C4: LOG(C4):
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    C6=C5/X C6: LOG(C6):
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    C8=C7/X C8: LOG(C8):