Synthesis and antioxidative activity of 2-substituted phenyl-5-(3'-indolyl)-oxazole derivatives / 药学学报
Acta Pharmaceutica Sinica
;
(12): 37-40, 2004.
Article
in English
| WPRIM
| ID: wpr-301153
ABSTRACT
<p><b>AIM</b>To study the synthesis of 5-(3'-indolyl)-oxazoles and their antioxidative activity.</p><p><b>METHODS</b>The amides were prepared from tryptophan and different acid derivatives by the catalytic dehydration of dicyclohexyl carbodiimide (DCC). The characteristic heterocyclic ring system of 5-(3'-indolyl)-oxazoles was constructed by oxidative cyclization of amide, using dicholorodicyanoquinone (DDQ). Their antioxidative activity in vitro was tested using DPPH system.</p><p><b>RESULTS</b>Eleven 2-substituted phenyl-5-(3'-indolyl)-oxazoles were prepared, the compounds 21 and 22 have shown antioxidative activity 3-4 times stronger than that of Vit E, and the compound 29 showed antioxidative activity almost as same as Vit E.</p><p><b>CONCLUSION</b>Three 5-(3'-indoyl)-oxazole compounds synthesized showed potent antioxidative effect and they would be a good antioxidants.</p>
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Oxazoles
/
Molecular Structure
/
Chemistry
/
Indoles
/
Antioxidants
Language:
English
Journal:
Acta Pharmaceutica Sinica
Year:
2004
Type:
Article
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