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The insulin secretory action of novel polycyclic guanidines: discovery through open innovation phenotypic screening, and exploration of structure-activity relationships.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2014 Feb 15; Vol. 24 (4), pp. 1031-6. Date of Electronic Publication: 2014 Jan 15. - Publication Year :
- 2014
-
Abstract
- We report the discovery of the glucose-dependent insulin secretogogue activity of a novel class of polycyclic guanidines through phenotypic screening as part of the Lilly Open Innovation Drug Discovery platform. Three compounds from the University of California, Irvine, 1-3, having the 3-arylhexahydropyrrolo[1,2-c]pyrimidin-1-amine scaffold acted as insulin secretagogues under high, but not low, glucose conditions. Exploration of the structure-activity relationship around the scaffold demonstrated the key role of the guanidine moiety, as well as the importance of two lipophilic regions, and led to the identification of 9h, which stimulated insulin secretion in isolated rat pancreatic islets in a glucose-dependent manner.<br /> (Copyright © 2014 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Subjects :
- Animals
Dose-Response Relationship, Drug
Glucose pharmacology
Guanidines chemical synthesis
Guanidines chemistry
Islets of Langerhans drug effects
Islets of Langerhans metabolism
Molecular Structure
Phenotype
Polycyclic Compounds chemical synthesis
Polycyclic Compounds chemistry
Rats
Structure-Activity Relationship
Drug Discovery
Guanidines pharmacology
Insulin metabolism
Polycyclic Compounds pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3405
- Volume :
- 24
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 24484900
- Full Text :
- https://doi.org/10.1016/j.bmcl.2014.01.021