clofibrate

Clofibrate (Clofibrato) 是芳氧基异丁酸衍生物，具有抗高血脂活性。它是一种 PPAR 的激动剂，对人和鼠 PPARα 和 PPARγ 的 EC50值分别为 55 μM，约500 μM 和 50 μM，约500 μM。

Etofylline clofibrate has a hypolipidemic and antithrombotic effect and it also has an agonistic interaction with intimal PGI2.

Aluminium clofibrate, a salt of clofibric acid, is a peroxisome proliferator.

Lysine clofibrate is a bioactive chemical.

Cinnarizine clofibrate is a calcium channel protein inhibitor as well as an antihistamine channel blocker. The compound is a drug derivative of piperazine. Cinnarizine is used for the control of vomiting due to motion sickness. It acts by interfering with the signal transmission between vestibular apparatus of the inner ear and the vomiting centre of the hypothalamus

Clofibrate mercapturate is a urinary metabolite of clofibrate.

Biclofibrate是一种抗血脂化合物，曾被研究用于降低血脂。

Clofibric acid (Chlorofibrinic acid) 是一种脂质纤维调节剂 Clofibrate，Etofibrate 和 Etofyllinclofibrate 的活性代谢物，是 PPARα的激动剂，具有降血脂作用，也可作为除草剂。

Picafibrate是clofibrate的衍生物，属于降低胆固醇的化合物。

Etofibrate 是烟酸和氯贝酸的醚二醇-1,2 二酯。它是动物和人类中一种有效的降血脂剂。

Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 50 µM in a transactivation assay) and the active metabolite of clofibrate. It is formed from clofibrate by tissue and serum esterases. Dietary administration of clofibric acid (0.067-0.22%) reduces serum cholesterol, phospholipid, and triglyceride levels in rats. It decreases glutamate oxaloacetate transaminase (GOT) levels and increases glutamate pyruvate transaminase (GPT) and lactate dehydrogenase (LDH) levels, markers of xenobiotic stress, in the plasma of carp (C. carpio) when administered in tank water at a concentration of 10 µg L. Clofibric acid has been found in wastewater effluent.

Sitofibrate, a clofibrate derivative, acts as a peroxisome proliferator-activated receptor-α (PPAR-α) agonist and serves as an antihyperlipidemic agent [1].