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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7699345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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