SYNTHESIS AND ANTIDIABETIC ACTIVITY OF THIAZOLO[2,3-f]PURINE DERIVATIVES AND THEIR ANALOGS

被引:5
作者
Spasov, A. A. [1 ]
Khaliullin, F. A. [2 ]
Babkov, D. A. [1 ]
Timirkhanova, G. A. [2 ]
Kuznetsova, V. A. [1 ]
Naumenko, L. V. [1 ]
Muleeva, D. R. [1 ]
Maika, O. Yu. [1 ]
Prokhorova, T. Yu. [1 ]
Sturova, E. A. [1 ]
机构
[1] Volgograd State Med Univ, Minist Hlth Russian Federat, Volgograd 400131, Russia
[2] Bashkir State Med Univ, Minist Hlth Russian Federat, Ufa 450008, Russia
基金
俄罗斯科学基金会;
关键词
thietanes; purine; antidiabetic activity; INHIBITORS; XANTHINE;
D O I
10.1007/s11094-017-1649-5
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:533 / 539
页数:7
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