Seladelpar sodium salt (Synonyms: MBX-8025 sodium salt; RWJ-800025 sodium salt) |
カタログ番号GC37622 |
Seladelpar ナトリウム塩 (MBX-8025) は、EC50 が 2 nM の経口活性、強力かつ特異的な PPARδ アゴニストであり、PPARα および PPARγ 受容体に対してそれぞれ 750 倍および 2500 倍以上の選択性を示します。
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Sample solution is provided at 25 µL, 10mM.
Seladelpar sodium salt (MBX-8025) is an orally active, potent and specific PPARδ agonist with an EC50 of 2 nM, showing more than 750-fold and 2500-fold selectivity over the PPARα and PPARγ receptors, respectively. PPAR-δ|2 nM (EC50)
MBX-8025 is an orally active, potent (EC50=2 nM), and specific (750-fold and 2500-fold compared with PPARα or PPARγ receptors, respectively) PPARδ agonist being developed as a lipid-altering agent[2][3].
In atherogenic diet-fed Wt mice, administration of Seladelpar sodium salt reduces body weight by ~18% (Pfoz/foz mice. Seladelpar sodium salt lowers serum alanine aminotransferase (ALT) levels in foz/foz mice (PWt mice. Seladelpar sodium salt normalizes serum cholesterol and decreases triglycerides in both genotypes (Pfoz/foz mice (P<0.05)[4].
[1]. Sahebkar A, et al. New peroxisome proliferator-activated receptor agonists: potential treatments for atherogenic dyslipidemia and non-alcoholic fatty liver disease. Expert Opin Pharmacother. 2014 Mar;15(4):493-503. [2]. Bays HE, et al. MBX-8025, a novel peroxisome proliferator receptor-delta agonist: lipid and other metabolic effects in dyslipidemic overweight patients treated with and without atorvastatin. J Clin Endocrinol Metab. 2011 Sep;96(9):2889-97. [3]. Choi YJ, et al. Effects of the PPAR-δ agonist MBX-8025 on atherogenic dyslipidemia. Atherosclerosis. 2012 Feb;220(2):470-6. [4]. Haczeyni F, et al. The selective peroxisome proliferator-activated receptor-delta agonist seladelpar reverses nonalcoholic steatohepatitis pathology by abrogating lipotoxicity in diabetic obese mice. Hepatol Commun. 2017 Jul 31;1(7):663-674.
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