Loading…

Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities

The synthesis of a library of new biaryl-based carbazoles bidentate directing group-assisted C-H functionalization and preliminary screening of the anticancer properties of biaryl-based carbazoles is reported. While various classes of modified carbazoles are known for their applications in materials...

Full description

Saved in:
Bibliographic Details
Published in:Organic & biomolecular chemistry 2024-11, Vol.22 (45), p.8916-8944
Main Authors: Kaur, Ramandeep, Dilip, Haritha, Kirubakaran, Sivapriya, Babu, Srinivasarao Arulananda
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c204t-5e017b6597683cbc42beb3a05c1769f9468fd8f49f8688a521f318f7879810043
container_end_page 8944
container_issue 45
container_start_page 8916
container_title Organic & biomolecular chemistry
container_volume 22
creator Kaur, Ramandeep
Dilip, Haritha
Kirubakaran, Sivapriya
Babu, Srinivasarao Arulananda
description The synthesis of a library of new biaryl-based carbazoles bidentate directing group-assisted C-H functionalization and preliminary screening of the anticancer properties of biaryl-based carbazoles is reported. While various classes of modified carbazoles are known for their applications in materials and medicinal chemistry, to our knowledge, the biological activities of designed biaryl-based carbazoles have been rarely known. Given the prominence of carbazoles in research in medicinal chemistry, we envisioned the scope for new scaffolds of carbazole-based biaryl structures. We screened the synthesized biaryl-based carbazoles for their anticancer properties against various cancer cell lines such as HeLa (cervical cancer), HCT116 (colon cancer), MDA-MB-231 and MDA-MB-468 (breast cancer). In addition, the hits were also tested in the human embryonic kidney cell line HEK293T to assess their impact on the viability of normal human cells in the presence of these compounds. In this preliminary study, we identified some of the biaryl-based carbazoles as lead compounds with anticancer activities.
doi_str_mv 10.1039/d4ob01392a
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3116676646</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3116676646</sourcerecordid><originalsourceid>FETCH-LOGICAL-c204t-5e017b6597683cbc42beb3a05c1769f9468fd8f49f8688a521f318f7879810043</originalsourceid><addsrcrecordid>eNpdkctKxDAUhoMojreNDyABNyJUkybNZanjFQZcqOuSpAlmaJsxaQedpzfjqAtX5z-c7_ycCwDHGF1gRORlQ4NGmMhSbYE9TDkvUEXk9p8u0QTspzRHCEvO6C6YEEkRFYzvge75sx_ebPIJBge1V_GzLbRKtoFGRa1WobUJLr2C0-IBurE3gw-9av1KrQVUfQPtx6INcZNnk2znYy4M3qje2Cxzz9IP3qZDsONUm-zRTzwAr3e3L9OHYvZ0_zi9mhWmRHQoKosw16zK0wpitKGltpooVBnMmXSSMuEa4ah0ggmhqhI7goXjgkuBEaLkAJxtfBcxvI82DXXnk7Ftq3obxlQTjBnjjFGW0dN_6DyMMW-4pr65UpaZOt9QJoaUonX1IvouH6vGqF4_ob6hT9ffT7jK8MmP5ag72_yhv1cnX5-bgaw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3131166292</pqid></control><display><type>article</type><title>Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities</title><source>Royal Society of Chemistry</source><creator>Kaur, Ramandeep ; Dilip, Haritha ; Kirubakaran, Sivapriya ; Babu, Srinivasarao Arulananda</creator><creatorcontrib>Kaur, Ramandeep ; Dilip, Haritha ; Kirubakaran, Sivapriya ; Babu, Srinivasarao Arulananda</creatorcontrib><description>The synthesis of a library of new biaryl-based carbazoles bidentate directing group-assisted C-H functionalization and preliminary screening of the anticancer properties of biaryl-based carbazoles is reported. While various classes of modified carbazoles are known for their applications in materials and medicinal chemistry, to our knowledge, the biological activities of designed biaryl-based carbazoles have been rarely known. Given the prominence of carbazoles in research in medicinal chemistry, we envisioned the scope for new scaffolds of carbazole-based biaryl structures. We screened the synthesized biaryl-based carbazoles for their anticancer properties against various cancer cell lines such as HeLa (cervical cancer), HCT116 (colon cancer), MDA-MB-231 and MDA-MB-468 (breast cancer). In addition, the hits were also tested in the human embryonic kidney cell line HEK293T to assess their impact on the viability of normal human cells in the presence of these compounds. In this preliminary study, we identified some of the biaryl-based carbazoles as lead compounds with anticancer activities.</description><identifier>ISSN: 1477-0520</identifier><identifier>ISSN: 1477-0539</identifier><identifier>EISSN: 1477-0539</identifier><identifier>DOI: 10.1039/d4ob01392a</identifier><identifier>PMID: 39404867</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Anticancer properties ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Cancer ; Carbazole ; Carbazoles ; Carbazoles - chemical synthesis ; Carbazoles - chemistry ; Carbazoles - pharmacology ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cervical cancer ; Chemical synthesis ; Colon cancer ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; HEK293 Cells ; Humans ; Lead compounds ; Molecular Structure ; Pharmaceutical sciences ; Structure-Activity Relationship ; Tumor cell lines</subject><ispartof>Organic &amp; biomolecular chemistry, 2024-11, Vol.22 (45), p.8916-8944</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c204t-5e017b6597683cbc42beb3a05c1769f9468fd8f49f8688a521f318f7879810043</cites><orcidid>0000-0002-7739-8200 ; 0000-0002-1795-8843 ; 0000-0002-7200-7602</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39404867$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kaur, Ramandeep</creatorcontrib><creatorcontrib>Dilip, Haritha</creatorcontrib><creatorcontrib>Kirubakaran, Sivapriya</creatorcontrib><creatorcontrib>Babu, Srinivasarao Arulananda</creatorcontrib><title>Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities</title><title>Organic &amp; biomolecular chemistry</title><addtitle>Org Biomol Chem</addtitle><description>The synthesis of a library of new biaryl-based carbazoles bidentate directing group-assisted C-H functionalization and preliminary screening of the anticancer properties of biaryl-based carbazoles is reported. While various classes of modified carbazoles are known for their applications in materials and medicinal chemistry, to our knowledge, the biological activities of designed biaryl-based carbazoles have been rarely known. Given the prominence of carbazoles in research in medicinal chemistry, we envisioned the scope for new scaffolds of carbazole-based biaryl structures. We screened the synthesized biaryl-based carbazoles for their anticancer properties against various cancer cell lines such as HeLa (cervical cancer), HCT116 (colon cancer), MDA-MB-231 and MDA-MB-468 (breast cancer). In addition, the hits were also tested in the human embryonic kidney cell line HEK293T to assess their impact on the viability of normal human cells in the presence of these compounds. In this preliminary study, we identified some of the biaryl-based carbazoles as lead compounds with anticancer activities.</description><subject>Anticancer properties</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Cancer</subject><subject>Carbazole</subject><subject>Carbazoles</subject><subject>Carbazoles - chemical synthesis</subject><subject>Carbazoles - chemistry</subject><subject>Carbazoles - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cervical cancer</subject><subject>Chemical synthesis</subject><subject>Colon cancer</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Screening Assays, Antitumor</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Lead compounds</subject><subject>Molecular Structure</subject><subject>Pharmaceutical sciences</subject><subject>Structure-Activity Relationship</subject><subject>Tumor cell lines</subject><issn>1477-0520</issn><issn>1477-0539</issn><issn>1477-0539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNpdkctKxDAUhoMojreNDyABNyJUkybNZanjFQZcqOuSpAlmaJsxaQedpzfjqAtX5z-c7_ycCwDHGF1gRORlQ4NGmMhSbYE9TDkvUEXk9p8u0QTspzRHCEvO6C6YEEkRFYzvge75sx_ebPIJBge1V_GzLbRKtoFGRa1WobUJLr2C0-IBurE3gw-9av1KrQVUfQPtx6INcZNnk2znYy4M3qje2Cxzz9IP3qZDsONUm-zRTzwAr3e3L9OHYvZ0_zi9mhWmRHQoKosw16zK0wpitKGltpooVBnMmXSSMuEa4ah0ggmhqhI7goXjgkuBEaLkAJxtfBcxvI82DXXnk7Ftq3obxlQTjBnjjFGW0dN_6DyMMW-4pr65UpaZOt9QJoaUonX1IvouH6vGqF4_ob6hT9ffT7jK8MmP5ag72_yhv1cnX5-bgaw</recordid><startdate>20241121</startdate><enddate>20241121</enddate><creator>Kaur, Ramandeep</creator><creator>Dilip, Haritha</creator><creator>Kirubakaran, Sivapriya</creator><creator>Babu, Srinivasarao Arulananda</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>7TM</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7739-8200</orcidid><orcidid>https://orcid.org/0000-0002-1795-8843</orcidid><orcidid>https://orcid.org/0000-0002-7200-7602</orcidid></search><sort><creationdate>20241121</creationdate><title>Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities</title><author>Kaur, Ramandeep ; Dilip, Haritha ; Kirubakaran, Sivapriya ; Babu, Srinivasarao Arulananda</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c204t-5e017b6597683cbc42beb3a05c1769f9468fd8f49f8688a521f318f7879810043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Anticancer properties</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Cancer</topic><topic>Carbazole</topic><topic>Carbazoles</topic><topic>Carbazoles - chemical synthesis</topic><topic>Carbazoles - chemistry</topic><topic>Carbazoles - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cervical cancer</topic><topic>Chemical synthesis</topic><topic>Colon cancer</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Screening Assays, Antitumor</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Lead compounds</topic><topic>Molecular Structure</topic><topic>Pharmaceutical sciences</topic><topic>Structure-Activity Relationship</topic><topic>Tumor cell lines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaur, Ramandeep</creatorcontrib><creatorcontrib>Dilip, Haritha</creatorcontrib><creatorcontrib>Kirubakaran, Sivapriya</creatorcontrib><creatorcontrib>Babu, Srinivasarao Arulananda</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Organic &amp; biomolecular chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaur, Ramandeep</au><au>Dilip, Haritha</au><au>Kirubakaran, Sivapriya</au><au>Babu, Srinivasarao Arulananda</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities</atitle><jtitle>Organic &amp; biomolecular chemistry</jtitle><addtitle>Org Biomol Chem</addtitle><date>2024-11-21</date><risdate>2024</risdate><volume>22</volume><issue>45</issue><spage>8916</spage><epage>8944</epage><pages>8916-8944</pages><issn>1477-0520</issn><issn>1477-0539</issn><eissn>1477-0539</eissn><abstract>The synthesis of a library of new biaryl-based carbazoles bidentate directing group-assisted C-H functionalization and preliminary screening of the anticancer properties of biaryl-based carbazoles is reported. While various classes of modified carbazoles are known for their applications in materials and medicinal chemistry, to our knowledge, the biological activities of designed biaryl-based carbazoles have been rarely known. Given the prominence of carbazoles in research in medicinal chemistry, we envisioned the scope for new scaffolds of carbazole-based biaryl structures. We screened the synthesized biaryl-based carbazoles for their anticancer properties against various cancer cell lines such as HeLa (cervical cancer), HCT116 (colon cancer), MDA-MB-231 and MDA-MB-468 (breast cancer). In addition, the hits were also tested in the human embryonic kidney cell line HEK293T to assess their impact on the viability of normal human cells in the presence of these compounds. In this preliminary study, we identified some of the biaryl-based carbazoles as lead compounds with anticancer activities.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>39404867</pmid><doi>10.1039/d4ob01392a</doi><tpages>29</tpages><orcidid>https://orcid.org/0000-0002-7739-8200</orcidid><orcidid>https://orcid.org/0000-0002-1795-8843</orcidid><orcidid>https://orcid.org/0000-0002-7200-7602</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1477-0520
ispartof Organic & biomolecular chemistry, 2024-11, Vol.22 (45), p.8916-8944
issn 1477-0520
1477-0539
1477-0539
language eng
recordid cdi_proquest_miscellaneous_3116676646
source Royal Society of Chemistry
subjects Anticancer properties
Antineoplastic Agents - chemical synthesis
Antineoplastic Agents - chemistry
Antineoplastic Agents - pharmacology
Cancer
Carbazole
Carbazoles
Carbazoles - chemical synthesis
Carbazoles - chemistry
Carbazoles - pharmacology
Cell Line, Tumor
Cell Proliferation - drug effects
Cell Survival - drug effects
Cervical cancer
Chemical synthesis
Colon cancer
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
HEK293 Cells
Humans
Lead compounds
Molecular Structure
Pharmaceutical sciences
Structure-Activity Relationship
Tumor cell lines
title Synthesis of biaryl-based carbazoles via C-H functionalization and exploration of their anticancer activities
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T18%3A43%3A37IST&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=Synthesis%20of%20biaryl-based%20carbazoles%20via%20C-H%20functionalization%20and%20exploration%20of%20their%20anticancer%20activities&rft.jtitle=Organic%20&%20biomolecular%20chemistry&rft.au=Kaur,%20Ramandeep&rft.date=2024-11-21&rft.volume=22&rft.issue=45&rft.spage=8916&rft.epage=8944&rft.pages=8916-8944&rft.issn=1477-0520&rft.eissn=1477-0539&rft_id=info:doi/10.1039/d4ob01392a&rft_dat=%3Cproquest_cross%3E3116676646%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c204t-5e017b6597683cbc42beb3a05c1769f9468fd8f49f8688a521f318f7879810043%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3131166292&rft_id=info:pmid/39404867&rfr_iscdi=true