PHENYL UREA ANALOGS AS FORMYL PEPTIDE REPCEPTOR 1 (FPR1) SELECTIVE AGONISTS

摘要

The present disclosure relates to phenyl urea derivatives, processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals as modulators of the N-formyl peptide receptor (FPR), such as agonism of the FPR1 and/or FPR2 receptor, or selective agonism of the FPR1 receptor relative to the FPR2 receptor.