A dual modulator of sEH and PPARγ
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RB394

Item No. 18909

Technical Information
Formal Name
α-ethyl-4-[[[[4-methoxy-2-(trifluoromethyl)phenyl]methyl]amino]carbonyl]-benzenepropanoic acid
CAS Number
1830320-32-5
Molecular Formula
C21H22F3NO4
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 25 mg/mlDMSO: 33 mg/mlDMSO:PBS (pH 7.2) (1:20): 0.04 mg/mlEthanol: 5 mg/ml
λmax
232, 280 nm
SMILES
COC1=CC(C(F)(F)F)=C(CNC(C2=CC=C(CC(C(O)=O)CC)C=C2)=O)C=C1
InChi Code
InChI=1S/C21H22F3NO4/c1-3-14(20(27)28)10-13-4-6-15(7-5-13)19(26)25-12-16-8-9-17(29-2)11-18(16)21(22,23)24/h4-9,11,14H,3,10,12H2,1-2H3,(H,25,26)(H,27,28)
InChi Key
VPAHYLNIDWFBPW-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    RB394 is an orally bioavailable, dual modulator of soluble epoxide hydrolase (sEH) and PPARγ that inhibits sEH with an IC50 of 0.33 µM and activates PPARγ with an EC50 of 0.3 µM.1 It is inactive at PPARδ and shows 29% activation of PPARα, relative to control, at 10 µM.1 RB394 is water soluble, orally bioavailable, and can be delivered through drinking water. In a two week in vivo pharmacokinetic study in mice, 30 mg/kg body weight in drinking water resulted in a final plasma concentration of ~3 µM.1 This coincided with upregulation of PPARγ target genes, as well as PPARα and PPARδ, in mouse livers.1

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Blöcher, R., Lamers, C., Wittman, S.K., et alN-benzylbenzamides: A novel merged scaffold for orally available dual soluble epoxide hydrolase/peroxisome proliferator-activated receptor γ modulators. J. Med. Chem. 59(1), 61-81 (2016).