Document Detail


Design and synthesis of N-(pyridylacryl) amino acid derivatives as potential radiosensitizers against HeLa-S3 cells in vitro.
MedLine Citation:
PMID:  7687084     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
A new series of N-(pyridylacryl) amino acid derivatives have been designed and synthesized as potential radiosensitizers in an effort to increase therapeutic efficacy with less toxicity. Radiosensitization and cytotoxicity of the newly synthesized compounds upon HeLa-S3 cells were measured. The main effects of the reduction of the shoulder width and Do value of the survival curve by 3-pyridylacrylsarcosine (3A) and 4-pyridylacrylsarcosine (4A) were observed. This work has demonstrated that this series of compounds, especially 3A and 4A, or their structurally related compounds, showed great clinical potential as radiosensitizers if significant radiosensitizing activity in vivo could be achieved.
Authors:
J Xin; B Hu; Z Li; F S Mi; Y Shen
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Yao xue xue bao = Acta pharmaceutica Sinica     Volume:  28     ISSN:  0513-4870     ISO Abbreviation:  Yao Xue Xue Bao     Publication Date:  1993  
Date Detail:
Created Date:  1993-08-11     Completed Date:  1993-08-11     Revised Date:  2004-11-17    
Medline Journal Info:
Nlm Unique ID:  21710340R     Medline TA:  Yao Xue Xue Bao     Country:  CHINA    
Other Details:
Languages:  eng     Pagination:  97-104     Citation Subset:  IM    
Affiliation:
Institute of Radiation Medicine, Chinese Academy of Medical Sciences, Tianjin.
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MeSH Terms
Descriptor/Qualifier:
Hela Cells
Humans
Pyridines / chemical synthesis*,  chemistry,  pharmacology
Radiation-Sensitizing Agents / chemical synthesis*,  chemistry,  pharmacology
Sarcosine / analogs & derivatives*,  chemical synthesis,  chemistry,  pharmacology
Chemical
Reg. No./Substance:
0/Pyridines; 0/Radiation-Sensitizing Agents; 107-97-1/Sarcosine; 148332-68-7/4-pyridylacrylsarcosine; 148332-70-1/3-pyridylacrylsarcosine

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