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Coumarin: A Natural, Privileged and Versatile Scaffold for Bioactive Compounds.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2018 Jan 27; Vol. 23 (2). Date of Electronic Publication: 2018 Jan 27. - Publication Year :
- 2018
-
Abstract
- Many naturally occurring substances, traditionally used in popular medicines around the world, contain the coumarin moiety. Coumarin represents a privileged scaffold for medicinal chemists, because of its peculiar physicochemical features, and the versatile and easy synthetic transformation into a large variety of functionalized coumarins. As a consequence, a huge number of coumarin derivatives have been designed, synthesized, and tested to address many pharmacological targets in a selective way, e.g., selective enzyme inhibitors, and more recently, a number of selected targets (multitarget ligands) involved in multifactorial diseases, such as Alzheimer's and Parkinson's diseases. In this review an overview of the most recent synthetic pathways leading to mono- and polyfunctionalized coumarins will be presented, along with the main biological pathways of their biosynthesis and metabolic transformations. The many existing and recent reviews in the field prompted us to make some drastic selections, and therefore, the review is focused on monoamine oxidase, cholinesterase, and aromatase inhibitors, and on multitarget coumarins acting on selected targets of neurodegenerative diseases.<br />Competing Interests: The authors declare no conflict of interest.
- Subjects :
- Alzheimer Disease drug therapy
Aromatase chemistry
Aromatase metabolism
Biotransformation
Cholinesterases chemistry
Cholinesterases metabolism
Coumarins pharmacology
Enzyme Inhibitors pharmacology
Humans
Molecular Structure
Monoamine Oxidase chemistry
Monoamine Oxidase metabolism
Neuroprotective Agents pharmacology
Nootropic Agents pharmacology
Parkinson Disease drug therapy
Structure-Activity Relationship
Coumarins chemical synthesis
Drug Design
Enzyme Inhibitors chemical synthesis
Neuroprotective Agents chemical synthesis
Nootropic Agents chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 23
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 29382051
- Full Text :
- https://doi.org/10.3390/molecules23020250