New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity

New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity

In order to obtain new compounds with antitumoural action the N-(metaacylaminobenzoyl)-α-acylaminobenzoyl)-α-aminoacids 4-9 were prepared. Thesecompounds were subsequently converted into the corresponding δ2-oxazolin-5-ones 10-15,which in turn were submitted to a ring opening reaction with...

Full description

Bibliographic Details
Main Authors: Lionte Catalina, Pintilie Otilia, Lenuta Profire, Jacques Desbrières, Marcel Popa, Valeriu Sunel
Format: Article
Language:English
Published: MDPI AG 2008-01-01
Series:Molecules
Subjects:
N-(acylaminobenzoyl)-α-aminoacids
Δ2-oxazolin-5-ones
anticancer agents
Online Access:http://www.mdpi.com/1420-3049/13/1/177/
Description
Summary:In order to obtain new compounds with antitumoural action the N-(metaacylaminobenzoyl)-α-acylaminobenzoyl)-α-aminoacids 4-9 were prepared. Thesecompounds were subsequently converted into the corresponding δ2-oxazolin-5-ones 10-15,which in turn were submitted to a ring opening reaction with di-(β-chloroethyl)amine toafford the peptide supported N-mustards 16-21, which showed low toxicity and cytostaticactivity similar to that of sarcolisine against the Ehrlich ascite and Walker 253carcinosarcoma.
ISSN:1420-3049

Similar Items