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BPK-25 Sale

目录号 : GC63510

BPK-25 是一种活性丙烯酰胺,通过涉及共价蛋白参与的翻译后机制促进核小体重塑和脱乙酰化 (NuRD) 复合蛋白的降解。BPK-25 通过环状二核苷酸配体 cGAMP 抑制 TMEM173 激活。

BPK-25 Chemical Structure

Cas No.:2305052-86-0

规格 价格 库存 购买数量
10mM (in 1mL DMSO)
¥2,970.00
现货
5 mg
¥2,700.00
现货
10 mg
¥4,410.00
现货
25 mg
¥8,820.00
现货
50 mg
¥13,500.00
现货

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Sample solution is provided at 25 µL, 10mM.

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BPK-25, an active acrylamide, promotes degradation of nucleosome remodeling and deacetylation (NuRD) complex proteins by a post-translational mechanism involving covalent protein engagement. BPK-25 inhibits TMEM173 activation by the cyclic dinucleotide ligand cGAMP[1].

BPK-25 (10 μM; 5 hours) inhibits TMEM173 activation by the cyclic dinucleotide ligand cGAMP[1]. BPK-25 (10 μM; 24 hours) suppresses NF-κB activation blocks nuclear factor of activated T-cells (NFAT) activation, as measured by >50% reductions in IκBα phosphorylation[1]. BPK-25 (10 μM; 4 hours) also reduces NFATc2 expression in T cells[1]. BPK-25 (0.1, 1, 5, 10, 20 μM; 24 hours) promotes the striking and selective reduction of several proteins in the nucleosome remodeling and deacetylation (NuRD) complex in a concentration- and time-dependent manner. BPK-25 does not have corresponding changes in mRNA expression[1]. A non-electrophilic propanamide analog of BPK-25 (BPK-25-ctrl) does not suppress T cell activation or affect NuRD complex proteins in T cells[1].

[1]. Ekaterina V Vinogradova, et al. An Activity-Guided Map of Electrophile-Cysteine Interactions in Primary Human T Cells. Cell. 2020 Aug 20;182(4):1009-1026.e29.

溶解性数据

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1 mg 5 mg 10 mg
1 mM 2.5456 mL 12.7278 mL 25.4557 mL
5 mM 0.5091 mL 2.5456 mL 5.0911 mL
10 mM 0.2546 mL 1.2728 mL 2.5456 mL
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