In silico consensus activity prediction, rational synthesis, and evaluation of antiglycation and antiplatelet activities of 3,6-disubstituted 1,2,4,5-tetrazines

According to the in silico consensus activity prediction, a series of 3,6-disubstituted 1,2,4,5-tetrazines were synthesized as promising inhibitors of the Maillard reaction. In addition to the studies of antiglycation activity, a comparative in vitro evaluation of the effect of the synthesized compo...

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Veröffentlicht in:Russian chemical bulletin 2020-04, Vol.69 (4), p.768-773
Hauptverfasser: Ishmetova, R. I., Babkov, D. A., Kucheryavenko, A. F., Babkova, V. A., Sirotenko, V. S., Ignatenko, N. K., Tolschina, S. G., Vassiliev, P. M., Rusinov, G. L., Spasov, A. A.
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container_issue 4
container_start_page 768
container_title Russian chemical bulletin
container_volume 69
creator Ishmetova, R. I.
Babkov, D. A.
Kucheryavenko, A. F.
Babkova, V. A.
Sirotenko, V. S.
Ignatenko, N. K.
Tolschina, S. G.
Vassiliev, P. M.
Rusinov, G. L.
Spasov, A. A.
description According to the in silico consensus activity prediction, a series of 3,6-disubstituted 1,2,4,5-tetrazines were synthesized as promising inhibitors of the Maillard reaction. In addition to the studies of antiglycation activity, a comparative in vitro evaluation of the effect of the synthesized compounds on the ADP-induced rabbit platelet aggregation model was carried out. Compounds with antiglycation and antiplatelet activities significantly higher than that of the reference drugs, aminoguanidine and acetylsalicylic acid, were revealed.
doi_str_mv 10.1007/s11172-020-2831-6
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subjects Acetylsalicylic acid
Chemistry
Chemistry and Materials Science
Chemistry/Food Science
Full Articles
Inorganic Chemistry
Maillard reaction
Organic Chemistry
title In silico consensus activity prediction, rational synthesis, and evaluation of antiglycation and antiplatelet activities of 3,6-disubstituted 1,2,4,5-tetrazines
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