Setogepram

Pharmaceutical compound From Wikipedia, the free encyclopedia

Setogepram (PBI-4050, Fezagepras) is an experimental drug which acts as a mixed agonist-antagonist for certain free fatty acid receptors, being an agonist at FFAR1 (GPR40) but an antagonist at GPR84. It has antiinflammatory and anti-fibrotic effects and has reached Phase II human clinical trials for treatment of idiopathic pulmonary fibrosis.[1][2][3][4][5]

Other namesPBI-4050, Fezagepras
CAS Number
Quick facts Clinical data, Other names ...
Setogepram
Clinical data
Other namesPBI-4050, Fezagepras
Identifiers
  • 2-(3-pentylphenyl)acetic acid
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
ChEMBL
Chemical and physical data
FormulaC13H18O2
Molar mass206.285 g·mol−1
3D model (JSmol)
  • CCCCCC1=CC(=CC=C1)CC(=O)O
  • InChI=1S/C13H18O2/c1-2-3-4-6-11-7-5-8-12(9-11)10-13(14)15/h5,7-9H,2-4,6,10H2,1H3,(H,14,15)
  • Key:PEGQOIGYZLJMIB-UHFFFAOYSA-N
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