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Uracil Hydroxybenzamides as Potential Antidiabetic Prodrugs
A series of N 1 , N 3 - bis -hydroxybenzoyl, -acetoxybenzoyl, and -methoxybenzoyl uracil derivatives were synthesized. All compounds were screened for the ability to rupture protein cross links and antiglycating, chelating, and antiaggregant properties, which are most significant for pharmacological...
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Published in: | Pharmaceutical chemistry journal 2019-09, Vol.53 (6), p.511-515 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A series of N
1
, N
3
-
bis
-hydroxybenzoyl, -acetoxybenzoyl, and -methoxybenzoyl uracil derivatives were synthesized. All compounds were screened for the ability to rupture protein cross links and antiglycating, chelating, and antiaggregant properties, which are most significant for pharmacological treatment of thrombosis and angio-, nephro-, encephalo-, and cardiopathies. 1,3-
bis
-(4-Methoxybenzoyl)pyrimidine-2,4(1
H
,3
H
)-dione was a promising antidiabetic agent with all studied activities. |
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ISSN: | 0091-150X 1573-9031 |
DOI: | 10.1007/s11094-019-02029-5 |