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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Main Authors: Francisco Valdés Zurita, Nelson Brown Vega, Margarita Gutiérrez Cabrera
Format: Article
Language:English
Published: MDPI AG 2018-05-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/23/5/1111
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spelling 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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