Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies

Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies

The design and synthesis of anthracene labeled bispyridinium amides 1-4 along with their anion binding, cell staining and DNA interaction studies are reported. All the chemosensors exhibit significant response towards H sub(2)PO sub(4) super(-) in CH sub(3)CN. Furthermore, sensors 2 and 3 are quite...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:New journal of chemistry 2012-01, Vol.36 (5), p.1231-1245
Hauptverfasser: Ghosh, Kumaresh, Sarkar, Avik Ranjan, Ghorai, Atanu, Ghosh, Utpal
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1245
container_issue 5
container_start_page 1231
container_title New journal of chemistry
container_volume 36
creator Ghosh, Kumaresh
Sarkar, Avik Ranjan
Ghorai, Atanu
Ghosh, Utpal
description The design and synthesis of anthracene labeled bispyridinium amides 1-4 along with their anion binding, cell staining and DNA interaction studies are reported. All the chemosensors exhibit significant response towards H sub(2)PO sub(4) super(-) in CH sub(3)CN. Furthermore, sensors 2 and 3 are quite interesting for the selective sensing of aliphatic dicarboxylates. Among these compounds, 1 is found to be useful in cell staining. Also all of them exhibit significant interaction with DNA. All these properties are found to be dependent on the nature of the spacer that holds the pyridinium binding sites.
doi_str_mv 10.1039/c2nj21024j
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1560118345</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1560118345</sourcerecordid><originalsourceid>FETCH-LOGICAL-c264t-b5d7b7e191e6afebd41d00ce74aefe6723cb83797be33e0f6b8ee105bf0980863</originalsourceid><addsrcrecordid>eNpFkM1OwzAQhC0EEqVw4Ql8RIiAHTtOwq1q-ZMquMA5suNN66pxitcR6tvjAhKn3Z39NBoNIZec3XIm6rs295ucs1xujsiEC1Vnda74cdq5lBkrpDolZ4gbxjgvFZ-QrwWgW3mqvaW493GdTqRDl4S4DroFD5nRCJYah7t9cNZ5N_ZU984C3ifMDT79fNJXN7SF7ZZi1Anyqx_TxeuMOh8hecUDinG0DvCcnHR6i3DxN6fk4_Hhff6cLd-eXuazZdbmSsbMFLY0JfCag9IdGCu5ZayFUmroQJW5aE0lyro0IASwTpkKgLPCdKyuWKXElFz9-u7C8DkCxqZ3eEipPQwjNrxQqYpKyCKh179oGwbEAF2zC67XYd9w1hzabf7bFd8wK2-2</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1560118345</pqid></control><display><type>article</type><title>Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>Ghosh, Kumaresh ; Sarkar, Avik Ranjan ; Ghorai, Atanu ; Ghosh, Utpal</creator><creatorcontrib>Ghosh, Kumaresh ; Sarkar, Avik Ranjan ; Ghorai, Atanu ; Ghosh, Utpal</creatorcontrib><description>The design and synthesis of anthracene labeled bispyridinium amides 1-4 along with their anion binding, cell staining and DNA interaction studies are reported. All the chemosensors exhibit significant response towards H sub(2)PO sub(4) super(-) in CH sub(3)CN. Furthermore, sensors 2 and 3 are quite interesting for the selective sensing of aliphatic dicarboxylates. Among these compounds, 1 is found to be useful in cell staining. Also all of them exhibit significant interaction with DNA. All these properties are found to be dependent on the nature of the spacer that holds the pyridinium binding sites.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/c2nj21024j</identifier><language>eng</language><ispartof>New journal of chemistry, 2012-01, Vol.36 (5), p.1231-1245</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c264t-b5d7b7e191e6afebd41d00ce74aefe6723cb83797be33e0f6b8ee105bf0980863</citedby><cites>FETCH-LOGICAL-c264t-b5d7b7e191e6afebd41d00ce74aefe6723cb83797be33e0f6b8ee105bf0980863</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Ghosh, Kumaresh</creatorcontrib><creatorcontrib>Sarkar, Avik Ranjan</creatorcontrib><creatorcontrib>Ghorai, Atanu</creatorcontrib><creatorcontrib>Ghosh, Utpal</creatorcontrib><title>Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies</title><title>New journal of chemistry</title><description>The design and synthesis of anthracene labeled bispyridinium amides 1-4 along with their anion binding, cell staining and DNA interaction studies are reported. All the chemosensors exhibit significant response towards H sub(2)PO sub(4) super(-) in CH sub(3)CN. Furthermore, sensors 2 and 3 are quite interesting for the selective sensing of aliphatic dicarboxylates. Among these compounds, 1 is found to be useful in cell staining. Also all of them exhibit significant interaction with DNA. All these properties are found to be dependent on the nature of the spacer that holds the pyridinium binding sites.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpFkM1OwzAQhC0EEqVw4Ql8RIiAHTtOwq1q-ZMquMA5suNN66pxitcR6tvjAhKn3Z39NBoNIZec3XIm6rs295ucs1xujsiEC1Vnda74cdq5lBkrpDolZ4gbxjgvFZ-QrwWgW3mqvaW493GdTqRDl4S4DroFD5nRCJYah7t9cNZ5N_ZU984C3ifMDT79fNJXN7SF7ZZi1Anyqx_TxeuMOh8hecUDinG0DvCcnHR6i3DxN6fk4_Hhff6cLd-eXuazZdbmSsbMFLY0JfCag9IdGCu5ZayFUmroQJW5aE0lyro0IASwTpkKgLPCdKyuWKXElFz9-u7C8DkCxqZ3eEipPQwjNrxQqYpKyCKh179oGwbEAF2zC67XYd9w1hzabf7bFd8wK2-2</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Ghosh, Kumaresh</creator><creator>Sarkar, Avik Ranjan</creator><creator>Ghorai, Atanu</creator><creator>Ghosh, Utpal</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope></search><sort><creationdate>20120101</creationdate><title>Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies</title><author>Ghosh, Kumaresh ; Sarkar, Avik Ranjan ; Ghorai, Atanu ; Ghosh, Utpal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c264t-b5d7b7e191e6afebd41d00ce74aefe6723cb83797be33e0f6b8ee105bf0980863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ghosh, Kumaresh</creatorcontrib><creatorcontrib>Sarkar, Avik Ranjan</creatorcontrib><creatorcontrib>Ghorai, Atanu</creatorcontrib><creatorcontrib>Ghosh, Utpal</creatorcontrib><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ghosh, Kumaresh</au><au>Sarkar, Avik Ranjan</au><au>Ghorai, Atanu</au><au>Ghosh, Utpal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies</atitle><jtitle>New journal of chemistry</jtitle><date>2012-01-01</date><risdate>2012</risdate><volume>36</volume><issue>5</issue><spage>1231</spage><epage>1245</epage><pages>1231-1245</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>The design and synthesis of anthracene labeled bispyridinium amides 1-4 along with their anion binding, cell staining and DNA interaction studies are reported. All the chemosensors exhibit significant response towards H sub(2)PO sub(4) super(-) in CH sub(3)CN. Furthermore, sensors 2 and 3 are quite interesting for the selective sensing of aliphatic dicarboxylates. Among these compounds, 1 is found to be useful in cell staining. Also all of them exhibit significant interaction with DNA. All these properties are found to be dependent on the nature of the spacer that holds the pyridinium binding sites.</abstract><doi>10.1039/c2nj21024j</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1144-0546
ispartof New journal of chemistry, 2012-01, Vol.36 (5), p.1231-1245
issn 1144-0546
1369-9261
language eng
recordid cdi_proquest_miscellaneous_1560118345
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Design and synthesis of anthracene-based bispyridinium amides: anion binding, cell staining and DNA interaction studies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T14%3A36%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design%20and%20synthesis%20of%20anthracene-based%20bispyridinium%20amides:%20anion%20binding,%20cell%20staining%20and%20DNA%20interaction%20studies&rft.jtitle=New%20journal%20of%20chemistry&rft.au=Ghosh,%20Kumaresh&rft.date=2012-01-01&rft.volume=36&rft.issue=5&rft.spage=1231&rft.epage=1245&rft.pages=1231-1245&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/c2nj21024j&rft_dat=%3Cproquest_cross%3E1560118345%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1560118345&rft_id=info:pmid/&rfr_iscdi=true