Cargando…

Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction

Polyethylene glycol (PEG) is a polymer that is widely used as a carrier for drug delivery systems (DDS). A library of N-PEGylated quinoline derivatives of PEG molecular weight 200 was prepared rapidly after the activation of PEGs using maleic anhydride. Quinoline with a polymer backbone is essential...

Descripción completa

Detalles Bibliográficos
Autores principales: GAIDHANE, Mahesh, GHATOLE, Ajay, LANJEWAR, Kushal, HATZADE, Kishor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763119/
https://www.ncbi.nlm.nih.gov/pubmed/33488247
http://dx.doi.org/10.3906/kim-2006-13
_version_ 1783627941929811968
author GAIDHANE, Mahesh
GHATOLE, Ajay
LANJEWAR, Kushal
HATZADE, Kishor
author_facet GAIDHANE, Mahesh
GHATOLE, Ajay
LANJEWAR, Kushal
HATZADE, Kishor
author_sort GAIDHANE, Mahesh
collection PubMed
description Polyethylene glycol (PEG) is a polymer that is widely used as a carrier for drug delivery systems (DDS). A library of N-PEGylated quinoline derivatives of PEG molecular weight 200 was prepared rapidly after the activation of PEGs using maleic anhydride. Quinoline with a polymer backbone is essential as new material. PEG is a water-soluble nonionic polymer approved by food and drug organizations for medicine applications. Because of its nontoxic grapheme, it is widely utilized in numerous biochemical, cosmetic, pharmaceutical, and industrialized applications. The modern SwissADME is a web tool that stretches free admittance to a pool of hasty, yet solid, clarifying models for physicochemical properties, pharmacokinetics, and therapeutic science. The present facile synthetic strategy can be a practical approach for incorporating polymeric carriers conjugated with drug moieties, either in the backbone of the polymer or as a terminal and pendant group on the polymer chains.
format Online
Article
Text
id pubmed-7763119
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher The Scientific and Technological Research Council of Turkey
record_format MEDLINE/PubMed
spelling pubmed-77631192021-01-22 Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction GAIDHANE, Mahesh GHATOLE, Ajay LANJEWAR, Kushal HATZADE, Kishor Turk J Chem Article Polyethylene glycol (PEG) is a polymer that is widely used as a carrier for drug delivery systems (DDS). A library of N-PEGylated quinoline derivatives of PEG molecular weight 200 was prepared rapidly after the activation of PEGs using maleic anhydride. Quinoline with a polymer backbone is essential as new material. PEG is a water-soluble nonionic polymer approved by food and drug organizations for medicine applications. Because of its nontoxic grapheme, it is widely utilized in numerous biochemical, cosmetic, pharmaceutical, and industrialized applications. The modern SwissADME is a web tool that stretches free admittance to a pool of hasty, yet solid, clarifying models for physicochemical properties, pharmacokinetics, and therapeutic science. The present facile synthetic strategy can be a practical approach for incorporating polymeric carriers conjugated with drug moieties, either in the backbone of the polymer or as a terminal and pendant group on the polymer chains. The Scientific and Technological Research Council of Turkey 2020-12-16 /pmc/articles/PMC7763119/ /pubmed/33488247 http://dx.doi.org/10.3906/kim-2006-13 Text en Copyright © 2020 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/ ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
GAIDHANE, Mahesh
GHATOLE, Ajay
LANJEWAR, Kushal
HATZADE, Kishor
Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title_full Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title_fullStr Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title_full_unstemmed Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title_short Innovational combination of hetero-bifunctional N-PEG quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and P-glycoprotein, cytochrome p450 enzyme activity prediction
title_sort innovational combination of hetero-bifunctional n-peg quinoline scaffolds derivatives with improved anticancer activity against breast and colon cancer cell lines and p-glycoprotein, cytochrome p450 enzyme activity prediction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763119/
https://www.ncbi.nlm.nih.gov/pubmed/33488247
http://dx.doi.org/10.3906/kim-2006-13
work_keys_str_mv AT gaidhanemahesh innovationalcombinationofheterobifunctionalnpegquinolinescaffoldsderivativeswithimprovedanticanceractivityagainstbreastandcoloncancercelllinesandpglycoproteincytochromep450enzymeactivityprediction
AT ghatoleajay innovationalcombinationofheterobifunctionalnpegquinolinescaffoldsderivativeswithimprovedanticanceractivityagainstbreastandcoloncancercelllinesandpglycoproteincytochromep450enzymeactivityprediction
AT lanjewarkushal innovationalcombinationofheterobifunctionalnpegquinolinescaffoldsderivativeswithimprovedanticanceractivityagainstbreastandcoloncancercelllinesandpglycoproteincytochromep450enzymeactivityprediction
AT hatzadekishor innovationalcombinationofheterobifunctionalnpegquinolinescaffoldsderivativeswithimprovedanticanceractivityagainstbreastandcoloncancercelllinesandpglycoproteincytochromep450enzymeactivityprediction