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  • T1415Gemfibrozil吉非罗齐;Jezil;CI-719;Lopid;Decrelip

    Gemfibrozil interacts with peroxisome proliferator-activated receptors (PPARalpha) resulting in PPARalpha-mediated stimulation of fatty acid oxidation and an increase in lipoprotein lipase (LPL) synthesis. Gemfibrozil is a fibric acid derivative with hypo

    价 格:¥电议型 号:T1415产 地:中国大陆

  • T1415GemfibrozilGemfibrozil,CI-719,Lopid

    Gemfibrozil interacts with peroxisome proliferator-activated receptors (PPARalpha) resulting in PPARalpha-mediated stimulation of fatty acid oxidation and an increase in lipoprotein lipase (LPL) synthesis. Gemfibrozil is a fibric acid derivative with hypo

    价 格:¥电议型 号:T1415产 地:美洲

  • T71306Gemfibrozil-d6;化合物 Gemfibrozil-d6Gemfibrozil-d6

    Gemfibrozil-d6 is intended for use as an internal standard for the quantification of gemfibrozil by GC- or LC-MS. Gemfibrozil is a peroxisome proliferator-activated reporter α and PPARγ agonist. In vivo, gemfibrozil reduces serum total cholesterol, triglyceride, and LDL levels in a rat model of high-cholesterol diet-induced hyperlipidemia. Gemfibrozil reduces atherosclerotic plaque area, superoxide production, and expression of the genes encoding the NF-κB subunit p65 and chemokine (C-C) motif l

    价 格:¥电议型 号:T71306产 地:中国大陆

  • T1415Gemfibrozil;吉非罗齐CI-719|||Jezil|||Decrelip|||Lopid;吉非罗齐|||CI-719|||Jezil|||Decrelip|||Lopid

    Gemfibrozil (CI-719) interacts with peroxisome proliferator-activated receptors (PPARalpha) resulting in PPARalpha-mediated stimulation of fatty acid oxidation and an increase in lipoprotein lipase (LPL) synthesis. Gemfibrozil is a fibric acid derivative with hypolipidemic effects. This enhances triglyceride-rich lipoprotein clearance and reduces the expression of apolipoprotein C-III (apoC-III). The reduction in hepatic production of apoC-III result in the subsequent reduction of serum levels o

    价 格:¥电议型 号:T1415产 地:中国大陆

  • T11387Gemfibrozil 1-O-β-glucuronide;化合物 T11387Gemfibrozil 1-O-β-glucuronide

    Gemfibrozil 1-O-β-Glucuronide, a metabolite of Gemfibrozil , is a potent and competitive P450 (CYP) isoform CYP2C8 inhibitor with an IC50 of 4.07 μM.

    价 格:¥电议型 号:T11387产 地:中国大陆

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