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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: | , , , , , , , |
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container_end_page | 515 |
container_issue | 6 |
container_start_page | 511 |
container_title | Pharmaceutical chemistry journal |
container_volume | 53 |
creator | Brel’, A. K. Spasov, A. A. Lisina, S. V. Popov, S. S. Kucheryavenko, A. F. Litvinov, R. A. Salaznikova, O. A. Rashchenko, A. I. |
description | 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. |
doi_str_mv | 10.1007/s11094-019-02029-5 |
format | article |
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H
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bis
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H
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H
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1
, N
3
-
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-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
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H
,3
H
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issn | 0091-150X 1573-9031 |
language | eng |
recordid | cdi_gale_infotracmisc_A606399798 |
source | Springer Nature |
subjects | Hypoglycemic agents Medicine Organic Chemistry Pharmacology/Toxicology Pharmacy Pyrimidines |
title | Uracil Hydroxybenzamides as Potential Antidiabetic Prodrugs |
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