Cargando…

Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method

In the proposed model, the gray interconnect degree method was employed to process the acute toxicity values of phthalate acid esters (PAEs) to green algae, daphnia, mysid, and fish (predicted by EPI Suite software) and to obtain the comprehensive characterization value of the multireceptor toxicity...

Descripción completa

Detalles Bibliográficos
Autores principales: CHEN, Xinyi, LI, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164199/
https://www.ncbi.nlm.nih.gov/pubmed/34104046
http://dx.doi.org/10.3906/kim-2008-38
_version_ 1783701065601908736
author CHEN, Xinyi
LI, Yu
author_facet CHEN, Xinyi
LI, Yu
author_sort CHEN, Xinyi
collection PubMed
description In the proposed model, the gray interconnect degree method was employed to process the acute toxicity values of phthalate acid esters (PAEs) to green algae, daphnia, mysid, and fish (predicted by EPI Suite software) and to obtain the comprehensive characterization value of the multireceptor toxicity effect (MTE) of PAEs. The 3D-QSAR pharmacophore model indicated that hydrophobic groups significantly affected the MTE of PAEs. Based on this, 16 PAEs derivative molecules with significantly decreased comprehensive characterization value (more than 10%) of the toxic effects of multireceptors were designed. Among them, 13 PAEs derivative molecules reduced the toxicity values (predicted by the EPI Suite software) of four receptor organisms to varying degrees. Finally, two derivative molecules from PAEs were screened and could exist stably in the environment. The derivative molecule’s reduced toxicity to the receptor was obtained through molecular docking methods and simulated the PAEs’ primary metabolic response pathways. The above research results break through the pharmacophore model’s limitation of only being suitable for the single effect of pollutants. Its application provides a new theoretical verification basis for expanding the multieffect pharmacophore model.
format Online
Article
Text
id pubmed-8164199
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Scientific and Technological Research Council of Turkey
record_format MEDLINE/PubMed
spelling pubmed-81641992021-06-07 Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method CHEN, Xinyi LI, Yu Turk J Chem Article In the proposed model, the gray interconnect degree method was employed to process the acute toxicity values of phthalate acid esters (PAEs) to green algae, daphnia, mysid, and fish (predicted by EPI Suite software) and to obtain the comprehensive characterization value of the multireceptor toxicity effect (MTE) of PAEs. The 3D-QSAR pharmacophore model indicated that hydrophobic groups significantly affected the MTE of PAEs. Based on this, 16 PAEs derivative molecules with significantly decreased comprehensive characterization value (more than 10%) of the toxic effects of multireceptors were designed. Among them, 13 PAEs derivative molecules reduced the toxicity values (predicted by the EPI Suite software) of four receptor organisms to varying degrees. Finally, two derivative molecules from PAEs were screened and could exist stably in the environment. The derivative molecule’s reduced toxicity to the receptor was obtained through molecular docking methods and simulated the PAEs’ primary metabolic response pathways. The above research results break through the pharmacophore model’s limitation of only being suitable for the single effect of pollutants. Its application provides a new theoretical verification basis for expanding the multieffect pharmacophore model. The Scientific and Technological Research Council of Turkey 2021-04-28 /pmc/articles/PMC8164199/ /pubmed/34104046 http://dx.doi.org/10.3906/kim-2008-38 Text en Copyright © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
CHEN, Xinyi
LI, Yu
Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title_full Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title_fullStr Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title_full_unstemmed Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title_short Toxicity remission of PAEs on multireceptors after molecular modification through a 3D-QSAR pharmacophore model coupled with a gray interconnect degree method
title_sort toxicity remission of paes on multireceptors after molecular modification through a 3d-qsar pharmacophore model coupled with a gray interconnect degree method
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164199/
https://www.ncbi.nlm.nih.gov/pubmed/34104046
http://dx.doi.org/10.3906/kim-2008-38
work_keys_str_mv AT chenxinyi toxicityremissionofpaesonmultireceptorsaftermolecularmodificationthrougha3dqsarpharmacophoremodelcoupledwithagrayinterconnectdegreemethod
AT liyu toxicityremissionofpaesonmultireceptorsaftermolecularmodificationthrougha3dqsarpharmacophoremodelcoupledwithagrayinterconnectdegreemethod