ChemicalBook--->CAS DataBase List--->1374516-07-0

1374516-07-0

1374516-07-0 Structure

1374516-07-0 Structure
IdentificationBack Directory
[Name]

TUG 891
[CAS]

1374516-07-0
[Synonyms]

TUG 891
CS-2448
TUG 891;TUG-891
4-[(4-Fluoro-4'-methyl[1,1'-biphenyl]-2-yl)methoxy]-benzenepropanoic acid
Benzenepropanoic acid, 4-[(4-fluoro-4'-methyl[1,1'-biphenyl]-2-yl)methoxy]-
[Molecular Formula]

C23H21FO3
[MDL Number]

MFCD22421654
[MOL File]

1374516-07-0.mol
[Molecular Weight]

364.41
Chemical PropertiesBack Directory
[Boiling point ]

540.8±50.0 °C(Predicted)
[density ]

1.199±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO:30.0(Max Conc. mg/mL);82.32(Max Conc. mM)
DMF:5.0(Max Conc. mg/mL);13.72(Max Conc. mM)
Ethanol:1.0(Max Conc. mg/mL);2.74(Max Conc. mM)
[form ]

Powder
[pka]

4.70±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Uses]

TUG 891 is a potent and selective GPR120 agonist as a new potential target for treatment of type 2 diabetes and metabolic diseases.
[Biological Activity]

TUG-891 is an orally activepotent and selective agonist for human long chain free fatty acid (FFA) receptor FFA4/GPR120 (pEC50 of receptor β-arrestin-2 recruitment = 7.36/FFA4 vs. 4.19/FFA1 HEK transfectants; pEC50 of calcium mobilization = 7.02/FFA4 vs. 5.30/FFA1 transfectants)while exhibiting no activity toward human short-chain FFA receptors FFA2/GPR43 and FFA3/GPR41. TUG-891 also exhibits potent partial agonist activity toward murine FFA4 (pEC50 = 7.7775% efficacy by β-arrestin-2 recruitment assay; pEC50 = 6.89 by calcium mobilization)albeit with a reduced selectivity over mFFA1 (pEC50 = 5.92 by β-arrestin-2 recruitment and 6.41 by by calcium mobilization). When administered via water intake (~20 mg/kg/day)TUG-891 is reported to reverse food intake increases and body weight gains among mice subjected to sleep fragmentationand significantly attenuate visceral white adipose tissue inflammation as well as insulin resistance.''TUG-891a GPR120 agonist he
[storage]

Store at RT
Spectrum DetailBack Directory
[Spectrum Detail]

TUG 891(1374516-07-0)1HNMR
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