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4°C, sealed storage, away from moisture
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货期:1-2天
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MedChemExpress LLC
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5 mg/10 mg/25 mg/50 mg/100 mg
| 规格: | 5 mg | 产品价格: | ¥500.0 |
|---|---|---|---|
| 规格: | 10 mg | 产品价格: | ¥800.0 |
| 规格: | 25 mg | 产品价格: | ¥1700.0 |
| 规格: | 50 mg | 产品价格: | ¥2800.0 |
| 规格: | 100 mg | 产品价格: | ¥4500.0 |
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PF-8380 hydrochloride
CAS No. : 2070015-01-7
MCE 国际站:PF-8380 hydrochloride
产品活性:PF-8380 hydrochloride 是一种有效的 autotaxin 抑制剂,体外酶实验和人类全血细胞实验中,IC50 分别为 2.8 nM 和 101 nM。
研究领域:Metabolic Enzyme/Protease
作用靶点:Phosphodiesterase (PDE)
In Vitro: PF-8380 also inhibits rat autotaxin with an IC50 of 1.16 nM with FS-3 substrate. Potency of PF-8380 is maintained when using enzyme produced from fetal fibroblasts used in combination with lysophosphatidyl choline (LPC) as a substrate. In human whole blood incubated with PF-8380 for 2 h, autotaxin is inhibited with an IC50 of 101 nM. Autotaxin (ATX), an enzyme with lysophospholipase D (lysoPLD) activity, catalyzes the production of lysophosphatidic acid (LPA) from lysophosphatidylcholine (LPC). Pre-treatment of GL261 and U87-MG cells with 1 μM PF-8380 followed by 4 Gy irradiation results in decreased clonogenic survival, decreases migration (33% in GL261; P=0.002 and 17.9% in U87-MG; P=0.012), decreases invasion (35.6% in GL261; P=0.0037 and 31.8% in U87-MG; P=0.002), and attenuates radiation-induced Akt phosphorylation.
In Vivo: The pharmacokinetic profile of PF-8380 is evaluated at an intravenous dose of 1 mg/kg and oral doses of 1 to 100 mg/kg out to 24 h. PF-8380 has mean clearance of 31 mL/min/kg, volume of distribution at steady state of 3.2 L/kg, and effective t1/2 of 1.2 h. Oral bioavailability is moderate, ranging from 43 to 83%. Plasma concentrations increased with single oral escalating doses, but Cmax increased at a rate that is approximately proportional to dose from 1 to 10 mg/kg and less than proportional to dose from 10 to 100 mg/kg. PF-8380 exposures estimated by area under the curve are approximately proportional to dose and linear up to 100 mg/kg. Plasma C16:0, C18:0, and C20:0 LPA levels are measured immediately after collection. Maximal reduction of LPA levels is observed by the 3 mg/kg dose at 0.5 h with all LPA returning at or above baseline at 24 h. Treatment with 10 mg/kg PF-8380 increases tumor-associated vascularity modestly by 20% (P=0.497). When compared to control, treatment of PF-8380 45 min before 4 Gy irradiation decreases vascularity by nearly 48% when compared to control (P=0.031) and by 65% when compared to mice that received radiation alone (P=0.011).
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文献和实验1SuoAc5J/PF6yv1GcZlVMply2VVbnZwH+h5RBi6lJV3Lzqkxbh7VMEMel0SptZS0vOZcrls1ZX/j0ixO2tbZbJ5iR/3rp27LCW1lYvD4Jer0hIJSUvZGDz4C8D7Kn+WQkxUNPdBNljxT8RgT2CQKqpsEdyjplGBCICEYGIQETgAEOgLqJYrvRbsVgQ0UuLZDZESgvOHR0KhlyIpEJFJBbNLZrTtmKLNKcJEeZaX3/ZMvmciCq
/uXVCW3HdXL18ifTlu30XJ58gzJEztLvK8cEkaAeExIjxI9lrvw1OH53j+8gWmTJsqeeRMnTwZxoaGaFC/PtatXSvF5kjaaHG3HjJsKN46vYmSL0fY9wgjZ5HIbiRl01VMUUGWnEK78gMfPGJJOhj0He/cSUzJlR/aLHwoZlsy+CgsfGTwDeblRSXw4sULtGjWBP379sEgMiQ9de68FDMjaq2UfyVcUE/QUcCAPj1Ro1oV3Ll5HcPIxsTF1RV37
); 广东省自然科学基金(No 980460); 广东省医学科研课题(A1998233);广州市科委基础项目(98-J-003-01) 刘金保(广州医学院病理生理教研室, 广东 广州 510182) 钟南山(广州医学院病理生理教研室, 广东 广州 510182) 李树浓(广州医学院病理生理教研室, 广东 广州 510182) [参 考 文 献] [1] Mosmann TR, Cherwinski H, Bond MW, et al.Two types of murine helper
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