Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1362749 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
A new structural class of DGAT1 inhibitors was discovered and the structure–activity relationship was explored. The pyrrolotriazine core of the original lead molecule was changed to a pyrrolopyridazine core providing an increase in potency. Further exploration resulted in optimization of the propyl group at C7 and the discovery that the ester at C6 could be replaced by five-membered heterocyclic rings. The analogs prepared have DGAT1 IC50 values ranging from >10 μM to 48 nM.
Graphical abstractA new structural class of DGAT1 inhibitors possessing a pyrrolopyridazine core has been discovered. The optimization of DGAT1 inhibitory activity and increase in selectivity over ACAT1 is described.Figure optionsDownload full-size imageDownload as PowerPoint slide