Skip to main content
Vai all'homepage della Commissione europea (si apre in una nuova finestra)
italiano it
CORDIS - Risultati della ricerca dell’UE
CORDIS
Contenuto archiviato il 2024-04-30

Synthesis of the manumycin family of antibiotics and novel ras farnesyl transferase inhibitors for cancer chemotherapy

Obiettivo



Inhibitors of the Ras farnesyl transferase (FTPase) enzyme have recently been shown to possess great potential as anti-cancer agents, particularly for colon and pancreatic carcinomas. Members of the manumycin family of aminoepoxycyclohexenone antibiotics act as potent and selective inhibitors of FTPase but these complex natural products seem to be too inaccessible and unstable to be useful chemotherapeutic agents. However, there is good evidence that synthetic aminoepoxycyclohexenones could be designed with the necessary stability and accessibility, while retaining the desirable biological properties. No synthetic approaches to manumycin analogues have been reported but preliminary studies in York have developed suitable methodology. The overall aim of this proposal is to extend this chemistry, and to develop chiral modifications, in order to prepare the natural products, and simplified analogues, for biological screening. Novel chemistry includes organometallic coupling reactions, the use of chiral acetals and Lewvis acids, and the stereocontrolled synthesis of complex polyenes.

Campo scientifico (EuroSciVoc)

Programma(i)

Argomento(i)

Invito a presentare proposte

Dati non disponibili

Meccanismo di finanziamento

RGI - Research grants (individual fellowships)

Coordinatore

UNIVERSITY OF YORK
Contributo UE
Nessun dato
Indirizzo
University Road
YO1 5DD YORK
Regno Unito
Costo totale
Nessun dato

Partecipanti (1)