ChemicalBook--->CAS DataBase List--->2253745-70-7

2253745-70-7

2253745-70-7 Structure

2253745-70-7 Structure
IdentificationBack Directory
[Name]

5-Butyl-4-phenyl-6-[4-(phenylmethoxy)phenyl]-2-pyrimidinamine
[CAS]

2253745-70-7
[Synonyms]

5-Butyl-4-phenyl-6-[4-(phenylmethoxy)phenyl]-2-pyrimidinamine
[Molecular Formula]

C27H27N3O
[MOL File]

2253745-70-7.mol
[Molecular Weight]

409.52
Chemical PropertiesBack Directory
[Boiling point ]

643.3±65.0 °C(Predicted)
[density ]

1.139±0.06 g/cm3(Predicted)
[solubility ]

Chloroform: 10 mg/ml; Ethanol: 10 mg/ml; Methyl Acetate: 1 mg/ml
[pka]

3.66±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
[Signal word ]

Danger
Hazard InformationBack Directory
[Description]

5-Butyl-4-phenyl-6-[4-(phenylmethoxy)phenyl]-2-pyrimidinamine is an inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1; IC50s = 117 and 60 nM for the human and mouse enzymes, respectively).1 It inhibits LPS-induced prostaglandin E2 (PGE2; ) production in mouse peritoneal cells (IC50 = 31 nM). In vivo, 5-Butyl-4-phenyl-6-[4-(phenylmethoxy)phenyl]-2-pyrimidinamine (25 mg/kg) reduces carrageenan-induced paw edema in rats.
[Uses]

mPGES1-IN-5 (compound 18) is a polysubstituted pyrimidine compound and a submicromolar PGE2 production inhibitor. It exerts its anti-inflammatory effect mainly by inhibiting mPGES-1 and has a significant inhibitory effect on the acute inflammation model in vivo.
[References]

1. Kal?ic, F., Kolman, V., Ajani, H., et al. Polysubstituted pyrimidines as mPGES-1 inhibitors: Discovery of potent inhibitors of PGE2 production with strong anti-inflammatory effects in carrageenan-induced rat paw edema ChemMedChem 15(15),1398-1407(2020).
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