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经验配方 CAS号 C₁₅H₁₄O₅ 60-82-2 描述 概述 A cell-permeable inhibtor of protein kinase C (IC50 = 20-50 µM). Activates Ca2+-activated K+ channels in amphibian myelinated nerve fibers at micromolar concentrations. An inhibitor of myo-inositol uptake. Also inhibits L-type Ca2+ channel activity. A potent inhibitor of 5′-iodothyronine deiodinase. Antagonist of prostaglandin F2α receptors linked to phospholipase C in astrocytes. 产品目录编号 524488 品牌系列 Calbiochem®
同义词 2ʹ,4ʹ,6ʹ-Trihydroxy-3-p-hydroxyphenylpropiophenone 参考 参考 Berry, G.T., et al. 1994. Pediat. Res. 35, 141.
Koh, D.S., et al. 1994. Neurosci. Lett. 165, 167.
Morreale de Escobar, G., et al. 1994. Endocrinology 134, 2410.
Prevarskaya, N., et al. 1994. Mol. Cell. Neurosci. 5, 699.
Kitanaka, J., et al. 1993. J. Neurochem. 60, 704.
Wang, X., et al. 1993. Biochem. J. 290, 249.
Benga, G., et al. 1992. Eur. J. Cell Biol. 59, 219.
Jordan, M.L., and Wright, J. 1991. J. Surg. Res. 50, 569.产品信息 CAS号 60-82-2 具有ATP竞争性 N 形式 White solid Hill配方 C₁₅H₁₄O₅ 化学配方 C₁₅H₁₄O₅ Molar Mass 274.3 可逆 N 结构配方图像 生物信息 主靶 PKC 主靶IC50 20-50 µM against protein kinase C 纯度 ≥97% by TLC 理化信息 细胞可渗透 Y 溶解度 Acetone, EtOH, or MeOH 安全信息 R相 R: 36/37/38
Irritating to eyes, respiratory system and skin.S相 S: 26-36
In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear suitable protective clothing.储存和货运信息 货运代码 Ambient Temperature Only
毒性 Irritant
储存 -20°C
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-20°C). Ethanol stock solutions are stable for up to 1 month at -20°C.
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