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...
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2008-01-01
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doaj-b2bb85ba409246fdb48a697707f844e22020-11-24T20:59:23ZengMDPI AGMolecules1420-30492008-01-0113117718910.3390/molecules13010177New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral ActivityLionte CatalinaPintilie OtiliaLenuta ProfireJacques DesbrièresMarcel PopaValeriu SunelIn 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.http://www.mdpi.com/1420-3049/13/1/177/N-(acylaminobenzoyl)-α-aminoacidsΔ2-oxazolin-5-onesanticancer agents |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lionte Catalina Pintilie Otilia Lenuta Profire Jacques Desbrières Marcel Popa Valeriu Sunel |
spellingShingle |
Lionte Catalina Pintilie Otilia Lenuta Profire Jacques Desbrières Marcel Popa Valeriu Sunel New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity Molecules N-(acylaminobenzoyl)-α-aminoacids Δ2-oxazolin-5-ones anticancer agents |
author_facet |
Lionte Catalina Pintilie Otilia Lenuta Profire Jacques Desbrières Marcel Popa Valeriu Sunel |
author_sort |
Lionte Catalina |
title |
New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity |
title_short |
New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity |
title_full |
New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity |
title_fullStr |
New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity |
title_full_unstemmed |
New Di-(β-chloroethyl)-α-amides on N-(meta-Acylaminobenzoyl)- D,L-aminoacid Supports with Antitumoral Activity |
title_sort |
new di-(ãžâ²-chloroethyl)-ãžâ±-amides on n-(meta-acylaminobenzoyl)- d,l-aminoacid supports with antitumoral activity |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2008-01-01 |
description |
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. |
topic |
N-(acylaminobenzoyl)-α-aminoacids Δ2-oxazolin-5-ones anticancer agents |
url |
http://www.mdpi.com/1420-3049/13/1/177/ |
work_keys_str_mv |
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