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SMIP004

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产品名称: SMIP004
产品型号: GOY-Y2943
产品展商: 谷研
产品文档: 无相关文档
发布时间:2023-05-04

简单介绍

SMIP004≥ 20.5 mg/mL in DMSO, ≥ 53.6 mg/mL in EtOH with ultrasonic


SMIP004  的详细介绍


性能参数

产品名称

SMIP004

规格

5mg 10mg 25mg 50mg

货号

GOY-Y2943

 含量

>98.00%

CAS

143360-00-3

别名

SMIP 004;SMIP-004

 

 

化学名

N-(4-butyl-2-methylphenyl)acetamide

分子式

C13H19NO

分子量

分子量 205.3

溶解度

≥ 20.5 mg/mL in DMSO, ≥ 53.6 mg/mL in EtOH with ultrasonic

储存条件

Store at -20°C

General tips

 

用途

仅供科研

价格

电询

详细内容

IC50 Value: 1.09 uM (MTT assay in LNCaP-S14 cells) [1] SMIP004 (N-(4-butyl-2-methyl-phenyl) acetamide) is a novel inducer of cancer-cell selective apoptosis of human prostate cancer cells. Unlike SMIP001, SMIP004 was found to downregulate SKP2 and to stabilize p27, although neither SMIP is a proteasome inhibitor. in vitro: Whereas SMIP012 and 016 were moderately toxic in normal fibroblasts, SMIPs 001 and 004 showed substantial cancer cell specificity being at least five times more potent in LNCaP-S14 than in IMR90 cells , treatment with either MG132 or SMIP004 increased p27 half-life to > 6 h [1]. Both SMIP001 and 004 led to a strong increase in the recruitment of p27 to CDK2, while SMIP001 also slightly increased coprecipitation of p21 (Figure 6c). SMIP004 also reduced the amounts of cyclins E and A retrieved with CDK2. This was paralleled by a marked downregulation of cyclins E and A upon SMIP004 treatment. SMIP004 decreased the levels of positive cell cycle regulators, upregulated cyclin-dependent kinase inhibitors, and resulted in G1 arrest, inhibition of colony formation in soft agar, and cell death [2]. in vivo: SMIP004 potently inhibits the growth of prostate and breast cancer xenografts in mice [2]. Clinical trial: N/A

 

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