GW 9578
GW 9578 Basic information
- Product Name:
- GW 9578
- Synonyms:
-
- GW 9578 Exclusive
- KYQNYMXQHLMADB-UHFFFAOYSA-N
- GW 9578
- Propanoic acid, 2-[[4-[2-[[[(2,4-difluorophenyl)amino]carbonyl]heptylamino]ethyl]phenyl]thio]-2-methyl-
- CAS:
- 247923-29-1
- MF:
- C26H34F2N2O3S
- MW:
- 492.6215664
- Mol File:
- 247923-29-1.mol
GW 9578 Chemical Properties
- Boiling point:
- 641.7±55.0 °C(Predicted)
- Density
- 1.21±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF:10.0(Max Conc. mg/mL);20.3(Max Conc. mM)
DMSO:10.0(Max Conc. mg/mL);20.3(Max Conc. mM)
DMSO:PBS (pH 7.2) (1:2):0.3(Max Conc. mg/mL);0.61(Max Conc. mM)
Ethanol:2.5(Max Conc. mg/mL);5.07(Max Conc. mM) - pka
- 3.77±0.10(Predicted)
- form
- Liquid
- color
- Colorless to light yellow
GW 9578 Usage And Synthesis
Uses
GW9578 is a subtype-selective PPARα agonist (EC50s of 5 and 50 nM for murine and human PPAR-α) with potent lipid-lowering activity[1][2].
IC 50
mouse PPARα: 5 nM (EC50); h-PPARα: 50 nM (EC50)
References
[1] P J Brown, et al. A ureido-thioisobutyric acid (GW9578) is a subtype-selective PPARalpha agonist with potent lipid-lowering activity. J Med Chem. 1999 Sep 23;42(19):3785-8. DOI:10.1021/jm9903601
[2] Alexandre Trifilieff, et al. PPAR-alpha and -gamma but not -delta agonists inhibit airway inflammation in a murine model of asthma: in vitro evidence for an NF-kappaB-independent effect. Br J Pharmacol. 2003 May;139(1):163-71. DOI:10.1038/sj.bjp.0705232
[3] Dallas C Jones, et al. Nuclear receptor peroxisome proliferator-activated receptor alpha (PPARalpha) is expressed in resting murine lymphocytes. The PPARalpha in T and B lymphocytes is both transactivation and transrepression competent. J Biol Chem. 2002 DOI:10.1074/jbc.M106908200
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