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受注:045-509-1970 |
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Synonyms | NSC 310038 | Storage (From the date of receipt) |
3 years -20°C powder 1 years -80°C in solvent |
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| 化学式 | C14H14ClN3O2S |
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| 分子量 | 323.8 | CAS No. | 50892-23-4 | ||||||||||||
| Solubility (25°C)* | 体外 | DMSO | 65 mg/mL (200.74 mM) | ||||||||||||
| Ethanol | 65 mg/mL (200.74 mM) | ||||||||||||||
| Water | Insoluble | ||||||||||||||
| 体内 (毎回新しく調製した物を用意してください) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
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| 製品説明 | WY-14643 (Pirinixic Acid, NSC 310038) is a potent and selective PPARα activator with an EC50 of 1.5 μM. |
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| in vitro | WY 14643 (10 μM) almost completely inhibits interleukin-1-induced production of interleukin-6 and prostaglandin and expression of cyclooxygenase-2 in aortic smooth-muscle cells, through repression of NF-κB signaling. [2] WY14643 (250 μM) reduces VCAM-1 expression levels significantly, to 52 % of TNF-α-stimulated human endothelial cells. Pretreatment of endothelial cells with WY 14643 (10 μM) before TNF-α stimulation reduces U937 cell adhesion by 50%. [3] |
| in vivo | WY 14643 (1 mg/kg i.v. bolus) administration at 30 min before left anterior descending occlusion, causes significant reduction in infarct size of ∼44% in rats subjected to regional myocardial ischemia (25 min) and reperfusion (2 h). [4] WY 14643 (3 mg/kg) lowers basal plasma levels of glucose, triglycerides (-16% vs. untreated), and leptin (-52%), and also muscle triglyceride (-34%) and total long-chain acyl-CoAs (LCACoAs) (-41%) in high fat-fed rats. WY14643 substantially reduces visceral fat weight and total liver triglyceride content without increasing body weight gain. WY14643 enhances whole body insulin sensitivity (clamp glucose infusion rate increases 35% and glucose disposals 22%, vs. untreated). WY 14643 enhances insulin-mediated muscle glucose metabolic index (Rg') in red (47%) and white (63%) muscles as well as in white adipose tissue (90%), and reduces muscle triglyceride and LCACoA accumulation. [5] |
| キナーゼアッセイ | PPAR activation assay | |
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| COS1 cells (3 × 105) are seeded into 9-cm-diameter plates in phenol red-free medium supplemented with 5% fetal calf serum stripped of endogenous steroid by treatment with dextran-coated charcoal. After 3 days the medium is replaced and CsCl purified plasmid DNA (10 μg) added by calcium phosphate precipitation. Each plate contains a CAT reporter gene (1 μg), an expression vector (PPAR, 1 μg), the β-galactosidase expression vector, PCH110 and pBluescribe M13 + DNA as a carrier (5 μg). Ligand (1000 × stocks in DMSO) is added 30 min after transfection. After a further 20 hr the cells are washed and fresh ligand added. After an additional 24 hr, cell extracts are prepared by three cycles of freeze-thawing and assayed forβ-galactosidase activity which is used to normalize the CAT assays. Extracts corresponding to 2 units of β-galactosidase activity are used for the CAT assay with 0.1 μCi of [14C]chloramphenicol (50 mCi/mmol) for 1 hr at 37 ℃. The acetylated chloramphenicol is separated by chromatography on silica gelTLC plates. The acetylated chloramphenicol is excised and counted in 5 mL of scintillation fluid. | ||
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Data from [Data independently produced by , , Diabetes, 2017, 66(8):2112-2123]
| Formononetin ameliorates depression-like behaviors through rebalancing microglia M1/M2 polarization and inhibiting NLRP3 inflammasome: involvement of activating PPARα-mediated autophagy [ Mol Med, 2025, 31(1):153] | PubMed: 40275171 |
| Overexpression of Apolipoprotein A-I Alleviates Insulin Resistance in MASLD Mice Through the PPARα Pathway [ Int J Mol Sci, 2025, 26(3)1051] | PubMed: 39940822 |
| Inhibition of ACOX1 enhances the therapeutic efficacy of obeticholic acid in treating non-alcoholic fatty liver disease and mitigates its lipotoxicity [ Front Pharmacol, 2024, 15:1366479] | PubMed: 38595921 |
| Inhibition of ACOX1 enhances the therapeutic efficacy of obeticholic acid in treating non-alcoholic fatty liver disease and mitigates its lipotoxicity [ Front Pharmacol, 2024, 15:1366479] | PubMed: 38595921 |
| mTORC2 Facilitates Liver Regeneration Through Sphingolipid-Induced PPAR-α-Fatty Acid Oxidation [ Cell Mol Gastroenterol Hepatol, 2022, 14(6):1311-1331] | PubMed: 35931382 |
| Oroxylin A ameliorates AKI-to-CKD transition through maintaining PPARα-BNIP3 signaling-mediated mitochondrial homeostasis [ Front Pharmacol, 2022, 13:935937] | PubMed: 36081929 |
| Overexpression CPT1A reduces lipid accumulation via PPARα/CD36 axis to suppress the cell proliferation in ccRCC [ Acta Biochim Biophys Sin (Shanghai), 2022, 54(2):220-231] | PubMed: 35130611 |
| Critical role of peroxisome proliferator-activated receptor α in promoting platelet hyperreactivity and thrombosis under hyperlipidemia [ Haematologica, 2021, 10.3324/haematol.2021.279770] | PubMed: 34615341 |
| PPARα agonist WY-14,643 enhances ethanol metabolism in mice: Role of catalase [ Free Radic Biol Med, 2021, 169:283-293] | PubMed: 33892114 |
| CircRNA hsa_circ_0110102 inhibited macrophage activation and hepatocellular carcinoma progression via miR-580-5p/PPARα/CCL2 pathway [ Aging (Albany NY), 2021, 13(8):11969-11987] | PubMed: 33891564 |
長期の保管のために-20°Cの下で製品を保ってください。
人間や獣医の診断であるか治療的な使用のためにでない。
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