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PF-04577806

更新时间:2025-08-26 20:09:11

PF-04577806结构式
PF-04577806结构式
品牌特惠专场
常用名 PF-04577806 英文名 PF-04577806
CAS号 1072100-81-2 分子量 495.62
密度 1.2±0.1 g/cm3 沸点 613.4±55.0 °C at 760 mmHg
分子式 C26H37N7O3 熔点 N/A
MSDS N/A 闪点 324.8±31.5 °C

 PF-04577806用途


PF-04577806是一种有效、选择性和ATP竞争性PKC抑制剂。PF-04577806对PKCα、PKCβI、PKCβII、PKCγ和PKCθ具有较强的抑制活性,其IC50s分别为2.4nm、8.1nm、6.9nm、45.9nm和29.5nm。PF-04577806可逆转糖尿病大鼠视网膜血管渗漏[1]。

 PF-04577806名称

英文名 PF-04577806
英文别名 更多

 PF-04577806生物活性

描述 PF-04577806是一种有效、选择性和ATP竞争性PKC抑制剂。PF-04577806对PKCα、PKCβI、PKCβII、PKCγ和PKCθ具有较强的抑制活性,其IC50s分别为2.4nm、8.1nm、6.9nm、45.9nm和29.5nm。PF-04577806可逆转糖尿病大鼠视网膜血管渗漏[1]。
相关类别
靶点

PKCα:2.4 nM (IC50)

PKCβI:8.1 nM (IC50)

PKCβII:6.9 nM (IC50)

PKCγ:45.9 nM (IC50)

PKCδ:586 nM (IC50)

PKCθ:29.5 nM (IC50)

PKCε:522 nM (IC50)

体外研究 PF-04577806(0.001-10μM;10分钟)抑制糖尿病大鼠视网膜裂解物中的PKC活性,IC50为0.18μM[1]。PF-04577806(0.12-10μM;预处理60分钟)抑制佛波酯醋酸盐刺激的Jurkat细胞ERK1/2磷酸化,IC50为0.28μM[1]。PF-04577806(0.001-10μM;预处理1h)抑制HEK293细胞中SHP2的磷酸化,IC50为5.8nm。PF-04577806浓度依赖性地抑制佛波酯醋酸盐刺激的HEK293细胞释放白细胞介素8,IC50为0.12μM[1]。PF-04577806(1μM;48 h)对人脐静脉内皮细胞显示低细胞毒性,剩余细胞活力为100.5%存活率[1]。Western Blot分析[1]细胞系:Jurkat T细胞浓度:0,0.12,0.37,1.11,3.33,10.0μM培养时间:预处理1小时结果:磷酸化ERK1/2呈剂量依赖性下降,但总ERK1/2无下降。
参考文献

[1]. Grant S, et, al. Discovery of a novel class of targeted kinase inhibitors that blocks protein kinase C signaling and ameliorates retinal vascular leakage in a diabetic rat model. Eur J Pharmacol. 2010 Feb 10;627(1-3):16-25.

 PF-04577806物理化学性质

密度 1.2±0.1 g/cm3
沸点 613.4±55.0 °C at 760 mmHg
分子式 C26H37N7O3
分子量 495.62
闪点 324.8±31.5 °C
精确质量 495.295776
LogP 2.02
蒸汽压 0.0±1.8 mmHg at 25°C
折射率 1.602

 PF-04577806英文别名

N-(5-{[(2S,5R)-2,5-Dimethyl-4-(tetrahydro-2H-pyran-4-ylmethyl)-1-piperazinyl]carbonyl}-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl)-2-pyridinecarboxamide
PF-04577806
2-Pyridinecarboxamide, N-[5-[[(2S,5R)-2,5-dimethyl-4-[(tetrahydro-2H-pyran-4-yl)methyl]-1-piperazinyl]carbonyl]-1,4,5,6-tetrahydro-6,6-dimethylpyrrolo[3,4-c]pyrazol-3-yl]-
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PF-04577806价格

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