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ResminostatCAS No. : 864814-88-0
MCE 國際站:Resminostat
產(chǎn)品活性:Resminostat (RAS2410; 4SC-201) 是一種有效的 HDAC1,HHDAC3 和 HDAC6 抑制劑,IC50 值分別為 42.5,50.1,71.8 nM,同時(shí)對(duì) HDAC8 有較弱的抑制作用,IC50 值為 877 nM。
研究領(lǐng)域:Cell Cycle/DNA Damage | Epigenetics
作用靶點(diǎn):HDAC
In Vitro: Resminostat (RAS2410; 4SC-201; 5 μM) induces histone acetylation in myeloma cells. Resminostat hydrochloride displays a substrate competitive binding mode with a mean Ki value of 27 nM. Resminostat hydrochloride (5 μM) induces histone hyperacetylation in myeloma cells. Resminostat inhibits cell growth, induces apoptosis and inhibits MM cell proliferation. Resminostat (5 μM) also modulates expression of bcl-2 family proteins and inhibits Akt pathway signalling downstream of Akt. Resminostat exerts synergistic activity against myeloma cells when combined with common and new anti-myeloma agents.
Resminostat inhibits cell growth in head and neck squamous cell carcinoma cell lines, with IC50s ranging from 0.775 μM to 1.572 μM (IC50 for SCC25: 0.775 μM; CAL27: 1.572 μM; and FaDu: 0.899 μM). Resminostat (1.25 and 2.5 μM) has a synergistic effect with irradiation on HNSCC cell lines. Resminostat in combination with cisplatin induces a downregulation of survivin. However, Resminostat shows no effect on Mcl-1 and p-AKT expression.
Resminostat reduces viability of HCC cells with the co-treatment of AZD-2014, with IC50s ranging from 0.89 ± 0.12 μM to 0.07 ± 0.01 μM.
相關(guān)產(chǎn)品:Trichostatin A | 4-Phenylbutyric acid | Valproic acid | Entinostat | Sulforaphane | Romidepsin | RGFP966 | Tasquinimod | Corin | Tacedinaline | Dacinostat | ITSA-1 | SIS17 | Tubastatin A Hydrochloride | WT-161 | Givinostat hydrochloride monohydrate | Pyroxamide | Scriptaid | BRD-6929 | Bufexamac | HDAC8-IN-1 | Sinapinic acid | Apicidin | BML-210 | HDACs/mTOR Inhibitor 1 | M344 | Droxinostat | CG347B
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