>>Signaling Pathways>> Chromatin/Epigenetics>> Epigenetic Reader Domain>>GSK 5959

GSK 5959

Catalog No.GC12440

GSK 5959는 IC50이 ~ 80nM인 강력하고 선택적인 세포 투과성 BRPF1 브로모도메인 억제제입니다.

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GSK 5959 Chemical Structure

Cas No.: 901245-65-6

Size 가격 재고 수량
10mg
US$139.00
재고 있음
50mg
US$417.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

GSK-5959 is a potent, selective and cell permeable BRPF1 bromodomain inhibitor with IC50 ~ 80 nM. Exhibits >100-fold selectivity for BRPF1 over a panel of 35 other bromodomains, including BRPF2/3 and BET family bromodomains.IC50 value: 80 nMTarget: BRPF1in vitro: GSK-5959 inhibits BRPF1 interaction with histone H3. A cellular protein interaction assay measuring the displacement of NanoLuc-tagged BRPF1 bromodomain from Halotagged histone H3 is employed to demonstrate GSK-5959 is cell permeability and disruption of chromatin binding with IC50 of 0.98 μM. GSK-5959 is used at 10 μM final concentration in various in vitro assays.

References:
[1]. Demont EH, et al. 1,3-Dimethyl Benzimidazolones Are Potent, Selective Inhibitors of the BRPF1 Bromodomain. (2014) ACS Med Chem Lett. 5(11):1190-1195.

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