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Identification of highly potent and selective PI3Kδ inhibitors
- Source :
- Bioorganicmedicinal chemistry letters. 27(13)
- Publication Year :
- 2017
-
Abstract
- Selective PI3Kδ inhibitors have recently been hypothesized to be appropriate immunosuppressive agents for the treatment of immunological disorders such as rheumatoid arthritis. However, few reports have highlighted molecules that are highly selective for PI3Kδ over the other PI3K isoforms. In this letter, isoform and kinome selective PI3Kδ inhibitors are presented. The Structural Activity Relationship leading to such molecules is outlined.
- Subjects :
- 0301 basic medicine
Gene isoform
Models, Molecular
Clinical Biochemistry
Pharmaceutical Science
Phosphatidylinositol 3-Kinases
Pharmacology
Biochemistry
03 medical and health sciences
Mice
Structure-Activity Relationship
0302 clinical medicine
Drug Discovery
medicine
Structure–activity relationship
Animals
Humans
Kinome
Molecular Biology
Protein Kinase Inhibitors
PI3K/AKT/mTOR pathway
Phosphoinositide-3 Kinase Inhibitors
Dose-Response Relationship, Drug
Molecular Structure
Chemistry
Organic Chemistry
Highly selective
medicine.disease
030104 developmental biology
030220 oncology & carcinogenesis
Rheumatoid arthritis
Molecular Medicine
Identification (biology)
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 27
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....faa6e633769aca402bfa7c285b9d57d2