SYNEUROUT

Total Synthesis of (2R)-Hydroxy-Norneomajucin and Biological Evaluation of Neurite Outgrowth

 Coordinatore UNIVERSITAET BASEL 

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Prof.
Nome: Marcel
Cognome: Mayor
Email: send email
Telefono: 41612671006

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 207˙928 €
 EC contributo 207˙928 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-03-01   -   2016-02-29

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITAET BASEL

 Organization address address: Petersplatz 1
city: BASEL
postcode: 4003

contact info
Titolo: Prof.
Nome: Marcel
Cognome: Mayor
Email: send email
Telefono: 41612671006

CH (BASEL) coordinator 207˙928.80

Mappa


 Word cloud

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multidisciplinary    disease    perform    alder    lab    diels    norneomajucin    natural    molecule    biological    host    gademann    university    neurotrophic    intermediates    mediated    plan    basel    switzerland    hydroxy    synthetic   

 Obiettivo del progetto (Objective)

Over the past century, there has been a worldwide escalation in the prevalence of neurodegenerative diseases, such as Alzheimer’s, Parkinson’s and Huntington’s disease. There are still no cures for these disorders and current therapeutics are only palliative. More recently, emerging therapeutic approaches have focused on maintaining neuronal function in these disease models with small molecules that possess neurotrophic properties. In this multidisciplinary proposal, we plan to complete the first total synthesis of (2R)-hydroxy-norneomajucin, confirm the neurotrophic activity of this natural product and evaluate advanced intermediates, and also initiate investigations into the biological target of this compound. The key transformation of our synthetic approach involves a Transannular Diels–Alder (TADA) reaction to establish the ABC ring system of the molecule in a single step. Assembly of the Diels-Alder precursor will be achieved through the combination of four basic fragments utilizing a Yamaguchi macrolactonization, Pd-mediated coupling, Horner-Wadsworth-Emmons olefination and an alkylation. All synthetic work will be performed at the host institution (Gademann Lab, University of Basel, Switzerland). With (2R)-hydroxy-norneomajucin and analogs in hand, we then plan to perform a NGF-mediated neurite outgrowth PC-12 cellular assay on the natural product and advanced intermediates at the host institution (Gademann Lab, University of Basel, Switzerland). In addition, we plan to perform HIP-HOP assays to elucidate the biological target of this molecule in collaboration with Dominic Hoepfner (NIBR Novartis Basel). The latter collaborative project will help to establish a working partnership between academia and industry in Europe. In general, this multidisciplinary proposal will contribute to European research and the transfer of knowledge acquired by the fellow while in the United States.

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