ChemicalBook--->CAS DataBase List--->343321-96-0

343321-96-0

343321-96-0 Structure

343321-96-0 Structure
IdentificationBack Directory
[Name]

ILUPZUOBHCUBKB-UHFFFAOYSA-N
[CAS]

343321-96-0
[Synonyms]

ILUPZUOBHCUBKB-UHFFFAOYSA-N
Propanoic acid, 2-methyl-2-[4-[[[[4-methyl-2-[4-(trifluoromethyl)phenyl]-5-thiazolyl]carbonyl]amino]methyl]phenoxy]-
lipid,LDLc,GW-590735,GW 590735,HDLc,Peroxisome proliferator-activated receptors,GW590735,PPAR,imbalance,Inhibitor,inhibit,triglycerides,dyslipidemia
[Molecular Formula]

C23H21F3N2O4S
[MDL Number]

MFCD12912339
[MOL File]

343321-96-0.mol
[Molecular Weight]

478.48
Chemical PropertiesBack Directory
[Melting point ]

130-131 °C(Solv: toluene (108-88-3))
[density ]

1.342±0.06 g/cm3(Predicted)
[solubility ]

DMF: 30 mg/ml
DMSO: 30 mg/ml
Ethanol: 30 mg/mlPBS (pH 7.2): 0.25 mg/ml
[form ]

Solid
[pka]

3.24±0.10(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

GW 590735 is a potent and selective PPARα agonist. GW 590735 showsEC50=4 nM on PPARα and at least 500-fold selectivity versus PPARδ and PPARγ. GW 590735 can be used for the research of dyslipidemia[1].
[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)[1].
GW 590735 (intravenous administration; 2.7 mg/kg; rat) treatment shows Cl, Vd, T1/2, and F% are 5 mL/min/kg, 1 L/kg, 2.4 hours and 47%, respectively[1].
GW 590735 (intravenous administration; 2 mg/kg; dog) treatment shows Cl, Vd, T1/2, and F% are 13 mL/min/kg, 2.8 L/kg, 2.6 hours and 85%, respectively[1].

[References]

[1] Sierra ML, et al. Substituted 2-[(4-aminomethyl)phenoxy]-2-methylpropionic acid PPARalpha agonists. 1. Discovery of a novel series of potent HDLc raising agents. J Med Chem. 2007;50(4):685-695. DOI:10.1021/jm058056x
Spectrum DetailBack Directory
[Spectrum Detail]

ILUPZUOBHCUBKB-UHFFFAOYSA-N(343321-96-0)1HNMR
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