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Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity

A series of bornyl derivatives of p-(benzyloxy)phenylpropionic acid were prepared, and their hypoglycemic activities were examined by an oral glucose tolerance test in mice. The results of this test revealed two compounds, 1 and 3, that can reduce the blood level of glucose similarly to reference co...

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Autores principales: Kuranov, Sergey, Luzina, Olga, Khvostov, Mikhail, Baev, Dmitriy, Kuznetsova, Darya, Zhukova, Nataliya, Vassiliev, Pavel, Kochetkov, Andrey, Tolstikova, Tatyana, Salakhutdinov, Nariman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699345/
https://www.ncbi.nlm.nih.gov/pubmed/33228030
http://dx.doi.org/10.3390/ph13110404
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author Kuranov, Sergey
Luzina, Olga
Khvostov, Mikhail
Baev, Dmitriy
Kuznetsova, Darya
Zhukova, Nataliya
Vassiliev, Pavel
Kochetkov, Andrey
Tolstikova, Tatyana
Salakhutdinov, Nariman
author_facet Kuranov, Sergey
Luzina, Olga
Khvostov, Mikhail
Baev, Dmitriy
Kuznetsova, Darya
Zhukova, Nataliya
Vassiliev, Pavel
Kochetkov, Andrey
Tolstikova, Tatyana
Salakhutdinov, Nariman
author_sort Kuranov, Sergey
collection PubMed
description A series of bornyl derivatives of p-(benzyloxy)phenylpropionic acid were prepared, and their hypoglycemic activities were examined by an oral glucose tolerance test in mice. The results of this test revealed two compounds, 1 and 3, that can reduce the blood level of glucose similarly to reference compound vildagliptin. Both compounds were tested in an experiment on mice with metabolic disorders: the C57BL/6(Ay) strain. Along with hypoglycemic properties, the two compounds showed different abilities to correct lipid metabolism disorders. In silico prediction revealed that the studied substances are most likely bifunctional multitarget hypoglycemic compounds whose mechanism of action is based on a pronounced reduction in insulin resistance and a strong incretin-mimetic effect. The difference in the size of effects of these compounds on biochemical parameters of blood in the experiment on C57BL/6(Ay) mice was in good agreement with the computational prediction of the priority ranking of biological targets for these compounds. These results indicate that bornyl derivatives of p-(benzyloxy)phenylpropionic acid have a good potential as new agents for diabetes mellitus treatment due to their hypoglycemic and lipid-normalizing properties.
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spelling pubmed-76993452020-11-29 Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity Kuranov, Sergey Luzina, Olga Khvostov, Mikhail Baev, Dmitriy Kuznetsova, Darya Zhukova, Nataliya Vassiliev, Pavel Kochetkov, Andrey Tolstikova, Tatyana Salakhutdinov, Nariman Pharmaceuticals (Basel) Article A series of bornyl derivatives of p-(benzyloxy)phenylpropionic acid were prepared, and their hypoglycemic activities were examined by an oral glucose tolerance test in mice. The results of this test revealed two compounds, 1 and 3, that can reduce the blood level of glucose similarly to reference compound vildagliptin. Both compounds were tested in an experiment on mice with metabolic disorders: the C57BL/6(Ay) strain. Along with hypoglycemic properties, the two compounds showed different abilities to correct lipid metabolism disorders. In silico prediction revealed that the studied substances are most likely bifunctional multitarget hypoglycemic compounds whose mechanism of action is based on a pronounced reduction in insulin resistance and a strong incretin-mimetic effect. The difference in the size of effects of these compounds on biochemical parameters of blood in the experiment on C57BL/6(Ay) mice was in good agreement with the computational prediction of the priority ranking of biological targets for these compounds. These results indicate that bornyl derivatives of p-(benzyloxy)phenylpropionic acid have a good potential as new agents for diabetes mellitus treatment due to their hypoglycemic and lipid-normalizing properties. MDPI 2020-11-19 /pmc/articles/PMC7699345/ /pubmed/33228030 http://dx.doi.org/10.3390/ph13110404 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kuranov, Sergey
Luzina, Olga
Khvostov, Mikhail
Baev, Dmitriy
Kuznetsova, Darya
Zhukova, Nataliya
Vassiliev, Pavel
Kochetkov, Andrey
Tolstikova, Tatyana
Salakhutdinov, Nariman
Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title_full Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title_fullStr Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title_full_unstemmed Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title_short Bornyl Derivatives of p-(Benzyloxy)Phenylpropionic Acid: In Vivo Evaluation of Antidiabetic Activity
title_sort bornyl derivatives of p-(benzyloxy)phenylpropionic acid: in vivo evaluation of antidiabetic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699345/
https://www.ncbi.nlm.nih.gov/pubmed/33228030
http://dx.doi.org/10.3390/ph13110404
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