• 介绍：

   Fenofibrate 是一种选择性的 PPARα 激动剂，EC50 为 30 μM。Fenofibrate 抑制细胞色素 P450 亚型, 对 CYP2C19，CYP2B6，CYP2C9，CYP2C8 和 CYP3A4 的 IC50 分别为 0.2，0.7，9.7，4.8 和 142.1 μM。

• 熔点： 81℃

• 溶解性： DMSO  :  250  mg/mL  (692.85  mM;  Need  ultrasonic)

• 储存条件： 2-8℃

• 注意：部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。

• 8. [4.4] Li Shuyu et al."In-situ sequential crystallization of fenofibrate and tristearin – Understanding the distribution of API in particles and stability of solid lipid microparticles from the perspective of crystallization."EUROPEAN JOURNAL OF PHARMACEUTICS AN

• 7. [IF=0.9] Lv J. et al."Preparation of Hollow Mesoporous Silica-Based Carriers for Loading and Release of Fenofibrate."RUSSIAN JOURNAL OF GENERAL CHEMISTRY".2024 Jan;94(1):193-203

• 6. [IF=9.8] ShuCheng Liu et al."Estimating the prevalence of dyslipidemia by measuring fenofibrate in 33 cities in China."SCIENCE OF THE TOTAL ENVIRONMENT.2024 Feb;912:169426

• 5. [IF=5.1] Ruoyue Huang et al."Metabolomics reveals that sulfotransferase 1 may regulate colchicine-induced liver injury."CHEMICO-BIOLOGICAL INTERACTIONS.2023 Dec;386:110776

• 4. [IF=3.614] Jingchun Sun et al."Screening the bioactive compound from Coptis chinensis inflorescence by immobilized Peroxisome proliferator activated receptor gamma."JOURNAL OF SEPARATION SCIENCE

• 3. [IF=6.543] Li Feng-Jiao et al."A Novel Method for Identifying Parkin Binding Agents in Complex Preparations of Herbal Medicines."Oxid Med Cell Longev. 2022;2022:3260243

• 2. [IF=4.451] Jie Gao et al."Ferulic acid targets ACSL1 to ameliorate lipid metabolic disorders in db/db mice."J Funct Foods. 2022 Apr;91:105009

• 1. 魏亚青,吕江维,任君刚,张文君,王立,王鹏光.非诺贝特/介孔二氧化硅的制备及缓释性能研究[J].应用化工,2020,49(07):1687-1692.

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本计算器可帮助您计算出特定溶液中溶质的质量、溶液浓度和体积之间的关系，公式为：

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

• pg ng μg mg g kg =
  fM pM nM μM mM M *
  nL μL mL L *