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Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors

To improve the in vivo antidepressant activity of previously reported serotonin (5-HT) and norepinephrine (NE) dual reuptake inhibitors, three series of arylamidine derivatives were designed and synthesized. The in vitro 5-HT and NE reuptake inhibitory activities of these compounds were evaluated, a...

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Autores principales: Wen, Hui, Qin, Wen, Yang, Guangzhong, Guo, Yanshen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385122/
https://www.ncbi.nlm.nih.gov/pubmed/30704101
http://dx.doi.org/10.3390/molecules24030497
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author Wen, Hui
Qin, Wen
Yang, Guangzhong
Guo, Yanshen
author_facet Wen, Hui
Qin, Wen
Yang, Guangzhong
Guo, Yanshen
author_sort Wen, Hui
collection PubMed
description To improve the in vivo antidepressant activity of previously reported serotonin (5-HT) and norepinephrine (NE) dual reuptake inhibitors, three series of arylamidine derivatives were designed and synthesized. The in vitro 5-HT and NE reuptake inhibitory activities of these compounds were evaluated, and compound II-5 was identified as the most potent 5-HT (IC(50) = 620 nM) and NE (IC(50) = 10 nM) dual reuptake inhibitor. Compound II-5 exhibited potent antidepressant activity in the rat tail suspension test and showed an acceptable safety profile in a preliminary acute toxicity test in mice. Our results show that these arylamidine derivatives exhibit potent 5-HT/NE dual reuptake inhibition and should be explored further as antidepressant drug candidates.
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spelling pubmed-63851222019-02-23 Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors Wen, Hui Qin, Wen Yang, Guangzhong Guo, Yanshen Molecules Article To improve the in vivo antidepressant activity of previously reported serotonin (5-HT) and norepinephrine (NE) dual reuptake inhibitors, three series of arylamidine derivatives were designed and synthesized. The in vitro 5-HT and NE reuptake inhibitory activities of these compounds were evaluated, and compound II-5 was identified as the most potent 5-HT (IC(50) = 620 nM) and NE (IC(50) = 10 nM) dual reuptake inhibitor. Compound II-5 exhibited potent antidepressant activity in the rat tail suspension test and showed an acceptable safety profile in a preliminary acute toxicity test in mice. Our results show that these arylamidine derivatives exhibit potent 5-HT/NE dual reuptake inhibition and should be explored further as antidepressant drug candidates. MDPI 2019-01-30 /pmc/articles/PMC6385122/ /pubmed/30704101 http://dx.doi.org/10.3390/molecules24030497 Text en © 2019 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
Wen, Hui
Qin, Wen
Yang, Guangzhong
Guo, Yanshen
Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title_full Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title_fullStr Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title_full_unstemmed Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title_short Design and Synthesis of Arylamidine Derivatives as Serotonin/Norepinephrine Dual Reuptake Inhibitors
title_sort design and synthesis of arylamidine derivatives as serotonin/norepinephrine dual reuptake inhibitors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385122/
https://www.ncbi.nlm.nih.gov/pubmed/30704101
http://dx.doi.org/10.3390/molecules24030497
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