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J Med Chem ; 64(12): 8053-8075, 2021 06 24.
Article in English | MEDLINE | ID: mdl-34080862

ABSTRACT

Starting from our previously described PI3Kγ inhibitors, we describe the exploration of structure-activity relationships that led to the discovery of highly potent dual PI3Kγδ inhibitors. We explored changes in two positions of the molecules, including macrocyclization, but ultimately identified a simpler series with the desired potency profile that had suitable physicochemical properties for inhalation. We were able to demonstrate efficacy in a rat ovalbumin challenge model of allergic asthma and in cells derived from asthmatic patients. The optimized compound, AZD8154, has a long duration of action in the lung and low systemic exposure coupled with high selectivity against off-targets.


Subject(s)
Asthma/drug therapy , Class Ib Phosphatidylinositol 3-Kinase/metabolism , Protein Kinase Inhibitors/therapeutic use , Sulfonamides/therapeutic use , Thiazoles/therapeutic use , Animals , Asthma/chemically induced , Class I Phosphatidylinositol 3-Kinases/metabolism , Crystallography, X-Ray , Humans , Leukocytes, Mononuclear/drug effects , Male , Molecular Structure , Ovalbumin , Phosphatidylinositol 3-Kinases/metabolism , Protein Binding , Protein Kinase Inhibitors/chemical synthesis , Protein Kinase Inhibitors/metabolism , Protein Kinase Inhibitors/pharmacokinetics , Rats, Inbred BN , Structure-Activity Relationship , Sulfonamides/chemical synthesis , Sulfonamides/metabolism , Sulfonamides/pharmacokinetics , Thiazoles/chemical synthesis , Thiazoles/metabolism , Thiazoles/pharmacokinetics
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