TANDEM

Developing Tandem Reaction Sequences for the Rapid Synthesis of Selected Bioactive Natural Products Followed by Parallel synthesis of analogue libraries and Biological Evaluation

 Coordinatore PANEPISTIMIO KRITIS 

 Organization address address: UNIVERSITY CAMPUS GALLOS
city: RETHIMNO
postcode: 74100

contact info
Titolo: Ms.
Nome: Eva
Cognome: Michelidaki
Email: send email
Telefono: -395935
Fax: -395910

 Nazionalità Coordinatore Greece [EL]
 Totale costo 45˙000 €
 EC contributo 45˙000 €
 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-2007-2-2-ERG
 Funding Scheme MC-ERG
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-04-30   -   2011-04-29

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    PANEPISTIMIO KRITIS

 Organization address address: UNIVERSITY CAMPUS GALLOS
city: RETHIMNO
postcode: 74100

contact info
Titolo: Ms.
Nome: Eva
Cognome: Michelidaki
Email: send email
Telefono: -395935
Fax: -395910

EL (RETHIMNO) coordinator 0.00

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 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

molecules    analogues    family    compounds    natural    diverse    structurally    synthesis   

 Obiettivo del progetto (Objective)

A proposal for the concise synthesis of a family of cytotoxic natural products obtained from Polythia Crassa is contained herein. The short and highly effcient synthesis accesses all the structurally diverse family members from two simple common precursors. The synthesis makes use of novel tandem reaction sequences to access these molecules. The molecules and their syntheses are amenable to the inclusion of structural modifications and libraries of structurally diverse analogues will therefore be made using parallel synthesis techniques. Natural and synthetic compounds will then be tested against a panel of human tumour cell lines allowing iterative redesign of analogues to be undertaken in order to hone the activity and pharmacokinetic profile of promising lead compounds.

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