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SW2_110A Sale

目录号 : GC62390

SW2_110A 是一种选择性 chromobox 8 chromodomain (CBX8 ChD) 抑制剂,Kd 为 800 nM。SW2_110A 在体外对 CBX8 ChD 的选择性比所有其他 CBX 旁系同源物低 5 倍。

SW2_110A Chemical Structure

规格 价格 库存 购买数量
5 mg
¥3,150.00
现货
10 mg
¥5,220.00
现货
25 mg
¥9,900.00
现货
50 mg
¥15,300.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

SW2_110A is a selective chromobox 8 chromodomain (CBX8 ChD) inhibitor with a Kd of 800 nM. SW2_110A shows minimal 5-fold selectivity for CBX8 ChD over all other CBX paralogs in vitro[1].

SW2_110A specifically inhibits the association of CBX8 with chromatin in cells and inhibits the proliferation of THP1 leukemia cells driven by the MLL-AF9 translocation (IC50 of 26 µM). In THP1 cells, SW2_110A treatment results in a significant decrease in the expression of MLL-AF9 target genes, including HOXA9[1].

[1]. Sijie Wang, et al. Optimization of Ligands Using Focused DNA-Encoded Libraries To Develop a Selective, Cell-Permeable CBX8 Chromodomain Inhibitor. ACS Chem Biol. 2020 Jan 17;15(1):112-131.

Chemical Properties

Cas No. SDF
分子式 C42H60N6O7 分子量 760.96
溶解度 DMSO : 125 mg/mL (164.27 mM; Need ultrasonic) 储存条件 Store at -20°C, protect from light, stored under nitrogen
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1 mM 1.3141 mL 6.5706 mL 13.1413 mL
5 mM 0.2628 mL 1.3141 mL 2.6283 mL
10 mM 0.1314 mL 0.6571 mL 1.3141 mL
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Research Update

Optimization of Ligands Using Focused DNA-Encoded Libraries To Develop a Selective, Cell-Permeable CBX8 Chromodomain Inhibitor

ACS Chem Biol 2020 Jan 17;15(1):112-131.PMID:31755685DOI:PMC7247616

Polycomb repressive complex 1 (PRC1) is critical for mediating gene expression during development. Five chromobox (CBX) homolog proteins, CBX2, CBX4, CBX6, CBX7, and CBX8, are incorporated into PRC1 complexes, where they mediate targeting to trimethylated lysine 27 of histone H3 (H3K27me3) via the N-terminal chromodomain (ChD). Individual CBX paralogs have been implicated as drug targets in cancer; however, high similarities in sequence and structure among the CBX ChDs provide a major obstacle in developing selective CBX ChD inhibitors. Here we report the selection of small, focused, DNA-encoded libraries (DELs) against multiple homologous ChDs to identify modifications to a parental ligand that confer both selectivity and potency for the ChD of CBX8. This on-DNA, medicinal chemistry approach enabled the development of SW2_110A, a selective, cell-permeable inhibitor of the CBX8 ChD. SW2_110A binds CBX8 ChD with a Kd of 800 nM, with minimal 5-fold selectivity for CBX8 ChD over all other CBX paralogs in vitro. SW2_110A specifically inhibits the association of CBX8 with chromatin in cells and inhibits the proliferation of THP1 leukemia cells driven by the MLL-AF9 translocation. In THP1 cells, SW2_110A treatment results in a significant decrease in the expression of MLL-AF9 target genes, including HOXA9, validating the previously established role for CBX8 in MLL-AF9 transcriptional activation, and defining the ChD as necessary for this function. The success of SW2_110A provides great promise for the development of highly selective and cell-permeable probes for the full CBX family. In addition, the approach taken provides a proof-of-principle demonstration of how DELs can be used iteratively for optimization of both ligand potency and selectivity.