10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping
Protected from light,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Übersicht
GW 590735 is a potent and selective PPARα agonist. GW 590735 shows EC 50 =4 nM on PPARα and at least 500-fold selectivity versus PPARδ and PPARγ. GW 590735 can be used for the research of dyslipidemia.
In Vivo
GW 590735 (0.5-5 mg/kg; orally twice a day for 5 days) is able to lower LDLc and triglycerides (TG) and increase HDL cholesterol in the Apo-A-I-transgenic mouse model (male C57BL/6 mice transgenic for human ApoA-I) . GW 590735 (intravenous administration; 2.7 mg/kg; rat) treatment shows Cl, Vd, T 1/2 , and F % are 5 mL/min/kg, 1 L/kg, 2.4 hours and 47%, respectively . GW 590735 (intravenous administration; 2 mg/kg; dog) treatment shows Cl, Vd, T 1/2 , and F % are 13 mL/min/kg, 2.8 L/kg, 2.6 hours and 85%, respectively . MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Specifications
Spezifikationen & Reinheit
10mM in DMSO
Biochemische und physiologische Mechanismen
GW 590735 is a potent and selective PPARα agonist. GW 590735 shows EC 50 =4 nM on PPARα and at least 500-fold selectivity versus PPARδ and PPARγ . GW 590735 can be used for the research of dyslipidemia.
Storage
Protected from light,Store at -80°C
Verschickt in
Dry ice packs + Cold packs
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
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