Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides. / Kuranov, S. O.; Blokhin, M. E.; Borisov, S. A. и др.
в: Russian Journal of Bioorganic Chemistry, Том 45, № 5, 01.09.2019, стр. 374-380.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Synthesis and Hypoglycemic Activity of Aryl(Hetaryl)Propenoic Cyanopyrrolidine Amides
AU - Kuranov, S. O.
AU - Blokhin, M. E.
AU - Borisov, S. A.
AU - Khvostov, M. V.
AU - Luzina, O. A.
AU - Salakhutdinov, N. F.
N1 - Publisher Copyright: © 2019, Pleiades Publishing, Ltd.
PY - 2019/9/1
Y1 - 2019/9/1
N2 - Abstract: A series of amides based on (2S)-cyanopyrrolidine and α, β-unsaturated aryl- and hetarylcarboxylic acids have been synthesized. The dependence of the hypoglycemic activity of compounds on the structure of the aromatic fragment has been studied in the oral glucose tolerance test in mice. Amides based on (E)-3-phenylprop-2-enoic and (E)-3-(4-methoxyphenyl)prop-2-enoic acids and (2S)-cyanopyrrolidine have been shown to significantly reduce blood glucose levels in mice. The observed hypoglycemic effect at a dose of 10 mg/kg is comparable to the effect of hypoglycemic drug vildagliptin.
AB - Abstract: A series of amides based on (2S)-cyanopyrrolidine and α, β-unsaturated aryl- and hetarylcarboxylic acids have been synthesized. The dependence of the hypoglycemic activity of compounds on the structure of the aromatic fragment has been studied in the oral glucose tolerance test in mice. Amides based on (E)-3-phenylprop-2-enoic and (E)-3-(4-methoxyphenyl)prop-2-enoic acids and (2S)-cyanopyrrolidine have been shown to significantly reduce blood glucose levels in mice. The observed hypoglycemic effect at a dose of 10 mg/kg is comparable to the effect of hypoglycemic drug vildagliptin.
KW - cyanopyrrolidine
KW - diabetes mellitus type 2
KW - hypoglycemic activity
KW - oral glucose tolerance test
KW - MECHANISM
KW - NATURAL-PRODUCTS
KW - INHIBITORS
KW - DERIVATIVES
UR - http://www.scopus.com/inward/record.url?scp=85073608016&partnerID=8YFLogxK
U2 - 10.1134/S1068162019050078
DO - 10.1134/S1068162019050078
M3 - Article
AN - SCOPUS:85073608016
VL - 45
SP - 374
EP - 380
JO - Russian Journal of Bioorganic Chemistry
JF - Russian Journal of Bioorganic Chemistry
SN - 1068-1620
IS - 5
ER -
ID: 21927158