PFI-1 (PF-6405761)

目录号: GC15375纯度: >99.50%同义词: PF06405761
A BET bromodomain inhibitor

PFI-1 (PF-6405761)
Cas No.: 1403764-72-6
规格价格库存数量操作
1mg¥123.00现货
1
5mg¥308.00现货
1
10mg¥560.00现货
1
50mg¥1,540.00现货
1
100mg¥2,800.00现货
1
10mM (in 1mL DMSO)¥339.00现货
1

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产品描述 Description

PFI-1 (PF-6405761) is a selective inhibitor of BET for Brd4 and Brd2 with IC50 value of 220 nM and 98 nM, respectively [1].
BET family are transcriptional regulators which consist of Brd2, Brd3, Brd4 and BRDT and play a pivotal role in cell proliferation, cell cycle progression, and apoptosis. It has been shown that Brd4 involves in the survival of many diverse tumors via promoting growth transcription and anti-apoptosis genes. It is well known that BET are epigenetic readers which selectively bind to acetylated lysine residues on histone tails and recently BET inhibitor emerged as important therapy in NUT midline carcinoma and several types of hematopoietic cancers [2, 3].
PFI-1 is a potent BET inhibitor and has a similar selectivity with the reported BET inhibitor JQ1. When tested with BEAS-2Bs cells, PFI-1 treatment markedly suppressed the release of IL-6 and CXCL8 induced by IL-1β/H2O2 by inhibiting Brd4 [4]. In leukaemic cell line MV4 which were sensitive to BET inhibitors, PFI-1 treatment induced cell cycle and apoptosis through function on Brd4 [1]. When tested with NET cell lines, administration of PFI-1 reduced cell proliferation by inhibiting BET activity at low concentrations of 100 nM–1 μM [5].
References:
[1].    Picaud, S., et al., PFI-1, a highly selective protein interaction inhibitor, targeting BET Bromodomains. Cancer Res, 2013. 73(11): p. 3336-46.
[2].    Perry, M.M., et al., BET bromodomains regulate TGF-beta-induced proliferation and cytokine release in asthmatic airway smooth muscle. J Biol Chem, 2015.
[3].    Yu, L., et al., Small-Molecule BET Inhibitors in Clinical and Preclinical Development and Their Therapeutic Potential. Curr Top Med Chem, 2015.
[4].    Khan, Y.M., et al., Brd4 is essential for IL-1beta-induced inflammation in human airway epithelial cells. PLoS One, 2014. 9(4): p. e95051.
[5].   Kate E Lines, et al., Epigenetic modifiers reduce proliferation of human neuroendocrine tumour cell lines. Endocrine Abstracts, 2013. 31: p149.

产品文档 Product Documents

Purity:>99.50%

化学性质Chemical Properties

CAS 号
1403764-72-6
同义词
PF06405761
化学名
2-methoxy-N-(3-methyl-2-oxo-1,4-dihydroquinazolin-6-yl)benzenesulfonamide
SMILES
CN1CC2=C(C=CC(=C2)NS(=O)(=O)C3=CC=CC=C3OC)NC1=O
分子式
C16H17N3O4S
分子量
347.39 g/mol
溶解性
≥ 128.4 mg/mL in DMSO
保存条件
Store at -20°C
General tips
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。
储备液的保存方式和期限:-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。
为了提高溶解度,请将管子加热至 37°C,然后在超声波浴中震荡一段时间。
Shipping Condition
评估样品解决方案:配备蓝冰进行发货。所有其他可用尺寸:配备 RT,或根据请求配备蓝冰。

计算工具摩尔浓度 / 稀释 / 分子量 / 单位换算 / 体内配方 / 溶解度

g/mol