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merck millipore,默克密理博,371825,GPCR-Helix 8 Signaling Inhibitor, JF5 - Calbiochem
产品名称:GPCR-Helix 8 Signaling Inhibitor, JF5 - Calbiochem
产品型号:371825
The GPCR-Helix 8 Signaling Inhibitor, JF5 controls the biological activity of GPCR-Helix 8. This small molecule/inhibitor is primarily used for Biochemicals applications.
merck millipore,默克密理博,371825,GPCR-Helix 8 Signaling Inhibitor, JF5 - Calbiochem
- 产品介绍
重要规格表
经验配方 C₁₇H₂₂N₂ • HI 描述 概述 A cell-permeable quinolinimine compound that acts as a selective, potent blocker of G-protein coupled receptors (GPCR) that contain a constrained eighth helix (H8). The inhibition is selective and blocks G-protein signaling mediated via Gαq, but not Gα12. A non-orthosteric antagonist of PAR1 (IC50 = 4 µM) that is shown to inhibit PAR1 and CCR-4 induced platelet aggregation without affecting PAR4 mediated aggregation. Shown to inhibit thrombus formation following vascular injury (IC50 ~1 mg/kg). Also acts as a potent, non-competitive blocker of α2A-adrenergic receptors (IC50 = 2.5 µM as shown by a decrease in 3H-yohimbine binding). 产品目录编号 371825 品牌系列 Calbiochem®
同义词 4-Pentyl-2,3-dihydro-1H-cyclopenta[b]quinolin-9-imine, HI, 4-Pentyl-1,2,3,4-tetrahydro-9H-cyclopenta[b]quinolin-9-imine, HI, GPCR-H8 Signaling Inhibitor, JF5 参考 参考 Dowal, L., et al. 2011. Proc. Natl. Acad. Sci. USA 108, 2951. 产品信息 形式 Off-white powder Hill配方 C₁₇H₂₂N₂ • HI 化学配方 C₁₇H₂₂N₂ • HI Molar Mass 382.3 吸湿 Hygroscopic
结构配方图像 生物信息 纯度 ≥92% by HPLC 理化信息 溶解度 DMSO 储存和货运信息 货运代码 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
毒性 Standard Handling
储存 +2°C to +8°C
避光 Protect from light
吸湿 Hygroscopic
无需冷冻 No
特殊指南 Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C. 包装信息 惰性气体下包装 Packaged under inert gas
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