Structure-based drug design for diagnosis and treatment of neurological diseases

COST Action CM1103

Structure-based drug design for diagnosis and treatment of neurological diseases:
dissecting and modulating complex function in the monoaminergic systems of the brain

WEBSITE DEVELOPMENT WORK IN PROGRESS

Welcome to the project website for COST Action CM1103. All official information about the Action CM1103 can be found on the COST website.

The purpose of this site is to inform the scientific community about our work and activities.
We promote collaboration and co-operation in drug discovery for diagnosing and modulating the function of the monoamine system in the brain that underlies or accompanies so many neuropathologies.

This Action was approved by COST Committee of Senior Officials  on 17/05/2011.

Entry into force: 22/06/2011

Start of Action: 28/11/2011

End of Action: 27/11/2015

Abstract

The therapy of neuropsychiatric disorders is limited by the high variability of symptoms and behavioural disturbances. Few drugs are available to address specific subsets of neurological/mental symptoms, and none to aid in diagnosis or to stop the progress of neurodegenerative disorders. Neurotransmitters such as dopamine and serotonin play a central role in the pathophysiology of major neuropsychiatric illnesses, such as anxiety and mood disorders, schizophrenia, autism-spectrum disorders, Parkinson's disease, epilepsy, and dementias. Neurotransmitter-binding proteins such as receptors, transporters and common metabolic enzymes are the starting points for development of tools to diagnose and drugs to treat specific clusters of symptoms. Structure-based drug design, synthetic chemistry and biological characterisation will inform the choice of lead compounds to treat select subsets of brain malfunction. This COST collaboration facilitates the cross-disciplinary interaction for discovery of promiscuous