@article{Spasov, A.A.2018-03-07,
author = { Spasov, A.A.,  Khaliullin, F.A.,  Babkov, D.A.,  Timirkhanova, G.A.,  Kuznetsova, V.A.,  Naumenko, L.V.,  Muleeva, D.R.,  Maika, O.Yu.,  Prokhorova, T.Yu.,  Sturova, E.A.},
title = {},
year = {2017},
doi = {10.1007/s11094-017-1649-5},
publisher = {NP «NEICON»},
abstract = {Thiazolo[2, 3-f]purine derivatives and their analogs – dihydrothiazolo[2, 3-f]purine, 7-(thietan-3-yl)purine,
and 8-(2-hydroxypropylthio)purine derivatives – were synthesized. The compounds synthesized here had no
effects on protein glycation reactions using glucose; they gave weak inhibition of glycogen phosphorylase;
they had no hemorheological activity. Substances with hypotensive activity greater than that of Dibazol were
found. A number of substances had hypoglycemic effects greater than those of chlorpropamide and Adebit.
Two compounds inhibited dipeptidylpeptidase-4, but were less active than reference agent vildagliptin.},
URL = {https://repo.bashgmu.ru/publication/1126},
eprint = {https://repo.bashgmu.ru/files/1283},
}