Discovery of Potent, Efficient, and Selective Inhibitors of Phosphoinositide 3-Kinase δ through a Deconstruction and Regrowth Approach.
J Med Chem
; 61(24): 11061-11073, 2018 12 27.
Article
in En
| MEDLINE
| ID: mdl-30532965
A deconstruction of previously reported phosphoinositide 3-kinase δ (PI3Kδ) inhibitors and subsequent regrowth led to the identification of a privileged fragment for PI3Kδ, which was exploited to deliver a potent, efficient, and selective lead series with a novel binding mode observed in the PI3Kδ crystal structure.
Full text:
1
Database:
MEDLINE
Main subject:
Structure-Activity Relationship
/
Enzyme Inhibitors
/
Phosphoinositide-3 Kinase Inhibitors
Limits:
Animals
Language:
En
Journal:
J Med Chem
Journal subject:
QUIMICA
Year:
2018
Type:
Article