货号	规格	价格	上海	北京	珠海	重庆	武汉
S89996-5mg买3赠1	98.50%	￥336.00 S89996-5mg ￥336.00 现货（买3赠1）	4 4	-	-	-	-
S89996-10mg买3赠1	98.50%	￥576.00 S89996-10mg ￥576.00 现货（买3赠1）	5 5	-	-	-	-
S89996-25mg促销	98.50%	￥1280.00 ￥1020.00 S89996-25mg ￥1020.00 现货	5 5	-	-	-	-
S89996-100mg促销	≥98%	￥3280.00 ￥2620.00 S89996-100mg ￥2620.00 2-3天	0 货期：2-3天	-	-	-	-

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产品描述：

Pyroxamide is an histone deacetylases (HDACs) inhibitor with antineoplastic properties ( HDAC1;IC50: 0.1-0.2 μM).

靶点：

Apoptosis;HDAC;Apoptosis; HDAC

体内研究：

Pyroxamide may be a useful agent for the treatment of malignancy and that induction of p21/WAF1 in transformed cells by pyroxamide may contribute to the antitumor effects of this agent

细胞实验：

HDAC1 enzyme assay, A MEL cell line expressing the epitope Flag-tagged HDAC1 was generated.HDAC1-Flag was affinity purified by immunoprecipitation using M2 anti-Flag antibody-coated agarose, followed by elution from the agarose using the Flag peptide.[3H]acetate-labeled cellular histones were prepared from MEL cells and were used as a substrate for the HDAC activity assay.Released [3H]acetic acid was quantified by scintillation counting.For inhibition studies, the enzyme preparations were preincubated with pyroxamide (10 to 100,000 nm) for 30 min at 4°C.

参考文献：

1. Butler L M , Webb Y , Agus D B , et al. Inhibition of transformed cell growth and induction of cellular differentiation by pyroxamide, an inhibitor of histone deacetylase[J]. Clinical Cancer Research, 2001, 7(4):962-970.

溶解性：

Soluble in DMSO

保存条件：

-20℃

配置溶液浓度参考：

	1mg	5mg	10mg
1 mM	3.769 ml	18.846 ml	37.692 ml
5 mM	0.754 ml	3.769 ml	7.538 ml
10 mM	0.377 ml	1.885 ml	3.769 ml
50 mM	0.075 ml	0.377 ml	0.754 ml

注意：

部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

参考文献

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