Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents
We describe the semisynthesis and biological effects of adenosine derivatives, which were anticipated to function as agonists for the A3 receptor. Molecular docking was used to select candidate compounds. Fifteen nucleoside derivatives were obtained through nucleophilic substitutions of the N6-posit...
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doaj-e13033c1b2c446769e75fabe47e2d0aa2020-11-24T22:28:07ZengMDPI AGMolecules1420-30492018-05-01235111110.3390/molecules23051111molecules23051111Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative AgentsFrancisco Valdés Zurita0Nelson Brown Vega1Margarita Gutiérrez Cabrera2Institute of Chemistry of Natural Resources, University of Talca, 3460000 Talca, ChileMedical School, University of Talca, 3460000 Talca, ChileInstitute of Chemistry of Natural Resources, University of Talca, 3460000 Talca, ChileWe describe the semisynthesis and biological effects of adenosine derivatives, which were anticipated to function as agonists for the A3 receptor. Molecular docking was used to select candidate compounds. Fifteen nucleoside derivatives were obtained through nucleophilic substitutions of the N6-position of the nucleoside precursor 6-chloropurine riboside by amines of different origin. All compounds were purified by column chromatography and further characterized by spectroscopic and spectrometric techniques, showing moderate yield. These molecules were then evaluated for their antiproliferative activity in human gastric cancer cells expressing the A3 receptor. We found that the compounds obtained have antiproliferative activity and that new structural modifications can enhance their biological activity. The ADME (Absorption, Distribution, Metabolism and Excretion) properties of the most active compounds were also evaluated theoretically.http://www.mdpi.com/1420-3049/23/5/1111nucleoside derivativesadenosinecancerantiproliferative activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Francisco Valdés Zurita Nelson Brown Vega Margarita Gutiérrez Cabrera |
spellingShingle |
Francisco Valdés Zurita Nelson Brown Vega Margarita Gutiérrez Cabrera Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents Molecules nucleoside derivatives adenosine cancer antiproliferative activity |
author_facet |
Francisco Valdés Zurita Nelson Brown Vega Margarita Gutiérrez Cabrera |
author_sort |
Francisco Valdés Zurita |
title |
Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents |
title_short |
Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents |
title_full |
Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents |
title_fullStr |
Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents |
title_full_unstemmed |
Semisynthesis, Characterization and Evaluation of New Adenosine Derivatives as Antiproliferative Agents |
title_sort |
semisynthesis, characterization and evaluation of new adenosine derivatives as antiproliferative agents |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2018-05-01 |
description |
We describe the semisynthesis and biological effects of adenosine derivatives, which were anticipated to function as agonists for the A3 receptor. Molecular docking was used to select candidate compounds. Fifteen nucleoside derivatives were obtained through nucleophilic substitutions of the N6-position of the nucleoside precursor 6-chloropurine riboside by amines of different origin. All compounds were purified by column chromatography and further characterized by spectroscopic and spectrometric techniques, showing moderate yield. These molecules were then evaluated for their antiproliferative activity in human gastric cancer cells expressing the A3 receptor. We found that the compounds obtained have antiproliferative activity and that new structural modifications can enhance their biological activity. The ADME (Absorption, Distribution, Metabolism and Excretion) properties of the most active compounds were also evaluated theoretically. |
topic |
nucleoside derivatives adenosine cancer antiproliferative activity |
url |
http://www.mdpi.com/1420-3049/23/5/1111 |
work_keys_str_mv |
AT franciscovaldeszurita semisynthesischaracterizationandevaluationofnewadenosinederivativesasantiproliferativeagents AT nelsonbrownvega semisynthesischaracterizationandevaluationofnewadenosinederivativesasantiproliferativeagents AT margaritagutierrezcabrera semisynthesischaracterizationandevaluationofnewadenosinederivativesasantiproliferativeagents |
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1725747770754596864 |