"目录号: HY-13909
Cell Cycle/DNA DamageEpigenetics-
RGFP966 是一种选择性的HDAC3抑制剂,IC50为 80 nM,浓度高达 15 μM时,对其他 HDAC 也没作用效果。
HDAC
相关产品
Trichostatin A-Panobinostat-Vorinostat-Entinostat-Mocetinostat-Belinostat-ACY-1215-Valproic acid sodium salt-Romidepsin-Quisinostat-Sodium Butyrate-Sirtinol-Chidamide-Parthenolide-TMP269-
生物活性
Description
RGFP966 is a selectiveHDAC3inhibitor with anIC50of 80 nM and no effective inhibition of any other HDAC at concentrations up to 15 μM.
IC50& Target
IC50: 80 nM (HDAC3)[1]
In Vitro
RGFP966 potently and selectively inhibits HDAC 3 with IC50of 0.21 μM in RAW 264.7 macrophages, while HDACs 1 (IC50=5.6 μM), 2 (9.7 μM) and 8 (>100 μM), indicating a good level of selectivity for HDAC 3. The mRNA levels of HDACs 1, 2 and 3 are not significantly affected by RGFP966 in RAW 264.7 macrophages, whereas the HDAC 1 and HDAC 2 protein levels are slightly, though significantly, reduced upon RGFP966 treatment. Moreover, RGFP966 significantly reduced the transcriptional activity of NF-κB p65, whereas NF-κB p65 acetylation and localization remain unaltered[2].
In Vivo
RGFP966 (10 and 25 mg/kg) treatment significantly improves body weight, rotarod performance and several measures of motor function in the open field locomoter test[3]. RGFP966 at a 10 mg/kg dose penetrates the blood-brain barrier into rat auditory cortex with typical pharmacokinetics, which together establish feasibility for the modulation of A1 plasticity due to action in the auditory cortex[4].
References
[1].Malvaez M, et al. HDAC3-selective inhibitor enhances extinction of cocaine-seeking behavior in a persistent manner. Proc Natl Acad Sci U S A. 2013 Feb 12;110(7):2647-52.
[2].Leus NG, et al. HDAC 3-selective inhibitor RGFP966 demonstrates anti-inflammatory properties in RAW 264.7 macrophages and mouse precision-cut lung slices by attenuating NF-κB p65 transcriptional activity. Biochem Pharmacol. 2016 May 15;108:58-74.
[3].Jia H, et al. The Effects of Pharmacological Inhibition of Histone Deacetylase 3 (HDAC3) in Huntington's Disease Mice. PLoS One. 2016 Mar 31;11(3):e0152498.
[4].Bieszczad KM, et al. Histone Deacetylase Inhibition via RGFP966 Releases the Brakes on Sensory Cortical Plasticity and the Specificity of Memory Formation. J Neurosci. 2015 Sep 23;35(38):13124-32.