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PMID: 12670534 Published · ppublish English Journal Article Review

Therapeutic potential of phosphoinositide 3-kinase inhibitors.

Chemistry & biology ·Vol. 10 ·No. 3 ·2003-03-00 ·Pages 207-13

Ward S, Sotsios Y, Dowden J, Bruce I, Finan P

Abstract

At least one Holy Grail for many academic researchers and pharmaceutical research divisions alike has been to identify therapeutically useful selective PI3K inhibitors. There are several different but closely related PI3Ks which are thought to have distinct biological roles. Until now, however, researchers have been frustrated by poor selectivity of the available pharmacological inhibitors, which are unable to distinguish the different isoforms of PI3K adequately. Fortunately, recently published work gives cause for optimism; there are now several patent specifications published that describe new PI3K inhibitors, including some that are more selective for the delta isoform of PI3K. Given the involvement of PI3Ks in a plethora of biological settings, such isoform-selective inhibitors may have immense potential use for the treatment of patients with inflammatory and autoimmune disorders as well as cancer and cardiovascular diseases.

MeSH Terms
Autoimmune Diseases/drug therapy,enzymology Cardiovascular Diseases/drug therapy,enzymology Enzyme Inhibitors/chemistry,pharmacology Humans Inflammation/drug therapy,enzymology Isoenzymes/antagonists & inhibitors Neoplasms/drug therapy,enzymology Phosphoinositide-3 Kinase Inhibitors Structure-Activity Relationship
Chemicals
Enzyme Inhibitors Isoenzymes Phosphoinositide-3 Kinase Inhibitors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Ward Stephen
Department of Pharmacy and Pharmacology, Bath University, Claverton Down, Bath, BA2 7AY, United Kingdom. s.g.ward@bath.ac.uk
Sotsios Yannis
Dowden James
Bruce Ian
Finan Peter
Article Info
Journal
Chemistry & biology
Abbr.
Chem Biol
ISSN
1074-5521
Published
2003-03-00
Pages
207-13
Language
English
Region
United States
NLM ID
9500160
Subset
IM
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