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merck millipore,默克密理博,344270,Forskolin, Coleus forskohlii - CAS 66575-29-9 - Calbiochem
产品名称:Forskolin, Coleus forskohlii - CAS 66575-29-9 - Calbiochem
产品型号:344270
The major cell-permeable diterpene isolated from the Indian plant Coleus forskohlii.
merck millipore,默克密理博,344270,Forskolin, Coleus forskohlii - CAS 66575-29-9 - Calbiochem
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经验配方 CAS号 C₂₂H₃₄O₇ 66575-29-9 描述 概述 The major cell-permeable diterpene isolated from the Indian plant Coleus forskohlii. At low doses, it acts as a positive inotropic agent. At higher doses, it serves as a hypotensive and vasodilatory agent due to its actions as a smooth muscle relaxant. No major side effects are observed at effective doses. Forskolins pharmacological activities are due to its activation of adenylate cyclase (EC50 = 4 µM), resulting in increased cAMP levels. The exact mechanism of forskolins positive inotropic effect is unknown but may be related to a cAMP-dependent increase in Na+ permeability that results in indirect augmentation of Ca2+ release. Inhibits MAP kinase in rat renal mesangial cells (IC50 = 25 µM). Also acts as a Hh pathway antagonist. Shown to inhibit apoptosis in cerebellar granule cells and to induce apoptosis in resting human B lymphocytes. 产品目录编号 344270 品牌系列 Calbiochem®
同义词 7β-Acetoxy-8,13-epoxy-1α,6β,9α-trihydroxy-labd-14-en-11-one, Colforsin 参考 参考 D'Orazio, J.A., et al. 2006. Nature 443, 340.
Noveen, A., et al. 1996. Biochem. Biophys. Res. Commun. 219, 180.
Galli, C., et al. 1995. J. Neurosci. 15, 1172.
Li, X., et al. 1995. Am. J. Physiol. 269, C986.
Lomo, J., et al. 1995. J. Immunol. 154, 1634.
Uneyama, H., et al. 1993. J. Biol. Chem. 268, 168.
Laurenza, A., et al. 1989. Trends Pharmacol. Sci. 10, 442.
Adashi, E.Y., and Resnick, C.E. 1986. J. Cell. Biochem. 31, 217.
Seamon, K.B., and Daly, J.W. 1986. Adv. Cyclic Nucleotide Protein Phosphorylation Res. 20, 1.
Huang, R., et al. 1982. Cyclic Nucleotide Res. 8, 385.
Metzger, H., and Lindner, E. 1981. IRCS Med. Sci. Biochem. Cardiovasc. System Pharmacol. 9, 99.产品信息 CAS号 66575-29-9 具有ATP竞争性 N 形式 White to off-white crystalline solid Hill配方 C₂₂H₃₄O₇ 化学配方 C₂₂H₃₄O₇ Molar Mass 410.5 可逆 N 结构配方图像 生物信息 主靶 Adenylate cyclase 主靶IC50 25 µM inhibiting MAP kinase in rat renal mesangial cells; EC50 = 4 µM for activation of adenylate cyclase 纯度 ≥99% by HPLC 理化信息 细胞可渗透 Y 溶解度 DMSO GHS安全信息 RTECS QL6150000 安全信息 R相 R: 21
Harmful in contact with skin.S相 S: 36
Wear suitable protective clothing.储存和货运信息 货运代码 Ambient Temperature Only
毒性 Harmful
储存 +15°C to +30°C
无需冷冻 No
特殊指南 Following reconstitution, store in the refrigerator (4°C). DMSO stock solutions are stable for up to 4 months at 4°C.
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