成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

返回ChemicalBook首頁>CAS數(shù)據(jù)庫列表>1357389-11-7

1357389-11-7

中文名稱 RGFP966
英文名稱 RGFP-966
CAS 1357389-11-7
分子式 C21H19FN4O
分子量 362.4
MOL 文件 1357389-11-7.mol
更新日期 2024/11/15 18:20:32
1357389-11-7 結(jié)構(gòu)式 1357389-11-7 結(jié)構(gòu)式

基本信息

中文別名
HDAC3抑制劑(RGFP966)
(2E)-N-(2-氨基-4-氟苯基)-3-[1-(3-苯基-2-丙烯-1-基)-1H-吡唑-4-基]-2-丙烯酰胺
英文別名
CS-871
RGFP966
RGFP-966
RGFP 966
(E/Z)-RGFP 966
RGFP966, >=98%
RGFP966
RGFP-966
(2E)-N-(2-Amino-4-fluorophenyl)-3-[1-(3-phenyl-2-propen-1-yl)-1H-pyrazol-4-yl]-2-propenamide
2-Propenamide, N-(2-amino-4-fluorophenyl)-3-[1-(3-phenyl-2-propen-1-yl)-1H-pyrazol-4-yl]-, (2E)-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)630.4±55.0 °C(Predicted)
密度1.19±0.1 g/cm3(Predicted)
儲存條件-20°C
溶解度可溶于 DMSO(高達(dá) 20 mg/ml)
酸度系數(shù)(pKa)11.58±0.70(Predicted)
形態(tài)固體
顏色米白色
穩(wěn)定性可在-20°C下的DMSO溶液保存長達(dá)1個(gè)月。
RGFP966價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2024/11/08HY-13909RGFP966
RGFP966
1357389-11-75mg900元
2024/11/08HY-13909RGFP966
RGFP966
1357389-11-710mM * 1mLin DMSO990元
2024/11/08HY-13909RGFP966
RGFP966
1357389-11-710mg1183元

常見問題列表

生物活性
RGFP966 是高選擇性的 HDAC3 抑制劑,IC50 為 80 nM,在 15 μM 時(shí)對其他 HDAC 無抑制作用。RGFP966 能夠透過血腦屏障 (BBB)。
靶點(diǎn)

HDAC3

80 nM (IC 50 )

體外研究

RGFP966 potently and selectively inhibits HDAC 3 with IC 50 of 0.21 μM in RAW 264.7 macrophages, while HDACs 1 (IC 50 =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.

體內(nèi)研究

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. 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.

"1357389-11-7" 相關(guān)產(chǎn)品信息
1268524-69-1 1222800-79-4 58880-19-6 49843-98-3