New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities

New series of 3-(3-trifluoromethylphenyl)-6-iodo-4(3 H )-quinazolinone derivatives bearing thiosemicarbazones, pyrazoles, azomethine moieties at C-2 were synthesized. The obtained products were screened for their expected anticancer activity against; human liver cancer cell line (HepG2), breast canc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Medicinal chemistry research 2018-02, Vol.27 (2), p.571-582
Hauptverfasser: Abbas, Samir Y., El-Bayouki, Khairy A. M., Basyouni, Wahid M., Mostafa, Eslam A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 582
container_issue 2
container_start_page 571
container_title Medicinal chemistry research
container_volume 27
creator Abbas, Samir Y.
El-Bayouki, Khairy A. M.
Basyouni, Wahid M.
Mostafa, Eslam A.
description New series of 3-(3-trifluoromethylphenyl)-6-iodo-4(3 H )-quinazolinone derivatives bearing thiosemicarbazones, pyrazoles, azomethine moieties at C-2 were synthesized. The obtained products were screened for their expected anticancer activity against; human liver cancer cell line (HepG2), breast cancer cell line (MCF-7) and human lung adenocarcinoma epithelial cell line (A549) tumor cell lines. Cytotoxicity of the synthesized compounds showed good IC 50 for some products in comparison with the standard drug, doxorubicin. On the other hand, antiviral activity of the synthesized products against H 5 N 1 showed moderate to weak activity compared to Zanamivir reference drug.
doi_str_mv 10.1007/s00044-017-2083-7
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2000307512</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2000307512</sourcerecordid><originalsourceid>FETCH-LOGICAL-c316t-dad27733f7c4dcb05af47dda1c656fdc2c70dd3ecf5bc5e312af224706c7cf9b3</originalsourceid><addsrcrecordid>eNp1kEtPwzAQhC0EEqXwA7hF4gIHw_oVF26oAoqE4AJny_UDUqVOaydB5dfjECROnHZWM7MrfQidErgkAPIqAQDnGIjEFGYMyz00IUJwPCMU9rOGrKmg7BAdpbQCYBK4mKD1s_sskouVS0XjC37OFhd421VBfzV1FZrgCpvdXrdV79JNkXah_XApp3Wwhet13WWrCUNZh7Zqu3UTf7xh66uo60KbQbX5xTE68LpO7uR3TtHb_d3rfIGfXh4e57dP2DBStthqS6VkzEvDrVmC0J5LazUxpSi9NdRIsJY548XSCMcI1Z5SLqE00vjrJZuis_HuJjbbzqVWrZouhvxS0QyKgRSE5hQZUyY2KUXn1SZWax13ioAaqKqRqspU1UBVydyhYyflbHh38e_y_6VvjqJ8hg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2000307512</pqid></control><display><type>article</type><title>New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities</title><source>SpringerLink (Online service)</source><creator>Abbas, Samir Y. ; El-Bayouki, Khairy A. M. ; Basyouni, Wahid M. ; Mostafa, Eslam A.</creator><creatorcontrib>Abbas, Samir Y. ; El-Bayouki, Khairy A. M. ; Basyouni, Wahid M. ; Mostafa, Eslam A.</creatorcontrib><description>New series of 3-(3-trifluoromethylphenyl)-6-iodo-4(3 H )-quinazolinone derivatives bearing thiosemicarbazones, pyrazoles, azomethine moieties at C-2 were synthesized. The obtained products were screened for their expected anticancer activity against; human liver cancer cell line (HepG2), breast cancer cell line (MCF-7) and human lung adenocarcinoma epithelial cell line (A549) tumor cell lines. Cytotoxicity of the synthesized compounds showed good IC 50 for some products in comparison with the standard drug, doxorubicin. On the other hand, antiviral activity of the synthesized products against H 5 N 1 showed moderate to weak activity compared to Zanamivir reference drug.</description><identifier>ISSN: 1054-2523</identifier><identifier>EISSN: 1554-8120</identifier><identifier>DOI: 10.1007/s00044-017-2083-7</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Adenocarcinoma ; Anticancer properties ; Antitumor activity ; Antiviral activity ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Breast cancer ; Cancer ; Cell Biology ; Cytotoxicity ; Derivatives ; Doxorubicin ; Epithelial cells ; Hepatocytes ; Liver ; Liver cancer ; Original Research ; Pharmacology/Toxicology ; Pyrazoles ; Quinazolinone ; Synthesis ; Toxicity ; Tumor cell lines ; Zanamivir</subject><ispartof>Medicinal chemistry research, 2018-02, Vol.27 (2), p.571-582</ispartof><rights>Springer Science+Business Media, LLC 2017</rights><rights>Copyright Springer Science &amp; Business Media 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-dad27733f7c4dcb05af47dda1c656fdc2c70dd3ecf5bc5e312af224706c7cf9b3</citedby><cites>FETCH-LOGICAL-c316t-dad27733f7c4dcb05af47dda1c656fdc2c70dd3ecf5bc5e312af224706c7cf9b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00044-017-2083-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00044-017-2083-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,41469,42538,51300</link.rule.ids></links><search><creatorcontrib>Abbas, Samir Y.</creatorcontrib><creatorcontrib>El-Bayouki, Khairy A. M.</creatorcontrib><creatorcontrib>Basyouni, Wahid M.</creatorcontrib><creatorcontrib>Mostafa, Eslam A.</creatorcontrib><title>New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities</title><title>Medicinal chemistry research</title><addtitle>Med Chem Res</addtitle><description>New series of 3-(3-trifluoromethylphenyl)-6-iodo-4(3 H )-quinazolinone derivatives bearing thiosemicarbazones, pyrazoles, azomethine moieties at C-2 were synthesized. The obtained products were screened for their expected anticancer activity against; human liver cancer cell line (HepG2), breast cancer cell line (MCF-7) and human lung adenocarcinoma epithelial cell line (A549) tumor cell lines. Cytotoxicity of the synthesized compounds showed good IC 50 for some products in comparison with the standard drug, doxorubicin. On the other hand, antiviral activity of the synthesized products against H 5 N 1 showed moderate to weak activity compared to Zanamivir reference drug.</description><subject>Adenocarcinoma</subject><subject>Anticancer properties</subject><subject>Antitumor activity</subject><subject>Antiviral activity</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Cell Biology</subject><subject>Cytotoxicity</subject><subject>Derivatives</subject><subject>Doxorubicin</subject><subject>Epithelial cells</subject><subject>Hepatocytes</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Original Research</subject><subject>Pharmacology/Toxicology</subject><subject>Pyrazoles</subject><subject>Quinazolinone</subject><subject>Synthesis</subject><subject>Toxicity</subject><subject>Tumor cell lines</subject><subject>Zanamivir</subject><issn>1054-2523</issn><issn>1554-8120</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kEtPwzAQhC0EEqXwA7hF4gIHw_oVF26oAoqE4AJny_UDUqVOaydB5dfjECROnHZWM7MrfQidErgkAPIqAQDnGIjEFGYMyz00IUJwPCMU9rOGrKmg7BAdpbQCYBK4mKD1s_sskouVS0XjC37OFhd421VBfzV1FZrgCpvdXrdV79JNkXah_XApp3Wwhet13WWrCUNZh7Zqu3UTf7xh66uo60KbQbX5xTE68LpO7uR3TtHb_d3rfIGfXh4e57dP2DBStthqS6VkzEvDrVmC0J5LazUxpSi9NdRIsJY548XSCMcI1Z5SLqE00vjrJZuis_HuJjbbzqVWrZouhvxS0QyKgRSE5hQZUyY2KUXn1SZWax13ioAaqKqRqspU1UBVydyhYyflbHh38e_y_6VvjqJ8hg</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Abbas, Samir Y.</creator><creator>El-Bayouki, Khairy A. M.</creator><creator>Basyouni, Wahid M.</creator><creator>Mostafa, Eslam A.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope></search><sort><creationdate>20180201</creationdate><title>New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities</title><author>Abbas, Samir Y. ; El-Bayouki, Khairy A. M. ; Basyouni, Wahid M. ; Mostafa, Eslam A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-dad27733f7c4dcb05af47dda1c656fdc2c70dd3ecf5bc5e312af224706c7cf9b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenocarcinoma</topic><topic>Anticancer properties</topic><topic>Antitumor activity</topic><topic>Antiviral activity</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Cell Biology</topic><topic>Cytotoxicity</topic><topic>Derivatives</topic><topic>Doxorubicin</topic><topic>Epithelial cells</topic><topic>Hepatocytes</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Original Research</topic><topic>Pharmacology/Toxicology</topic><topic>Pyrazoles</topic><topic>Quinazolinone</topic><topic>Synthesis</topic><topic>Toxicity</topic><topic>Tumor cell lines</topic><topic>Zanamivir</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abbas, Samir Y.</creatorcontrib><creatorcontrib>El-Bayouki, Khairy A. M.</creatorcontrib><creatorcontrib>Basyouni, Wahid M.</creatorcontrib><creatorcontrib>Mostafa, Eslam A.</creatorcontrib><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Medicinal chemistry research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abbas, Samir Y.</au><au>El-Bayouki, Khairy A. M.</au><au>Basyouni, Wahid M.</au><au>Mostafa, Eslam A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities</atitle><jtitle>Medicinal chemistry research</jtitle><stitle>Med Chem Res</stitle><date>2018-02-01</date><risdate>2018</risdate><volume>27</volume><issue>2</issue><spage>571</spage><epage>582</epage><pages>571-582</pages><issn>1054-2523</issn><eissn>1554-8120</eissn><abstract>New series of 3-(3-trifluoromethylphenyl)-6-iodo-4(3 H )-quinazolinone derivatives bearing thiosemicarbazones, pyrazoles, azomethine moieties at C-2 were synthesized. The obtained products were screened for their expected anticancer activity against; human liver cancer cell line (HepG2), breast cancer cell line (MCF-7) and human lung adenocarcinoma epithelial cell line (A549) tumor cell lines. Cytotoxicity of the synthesized compounds showed good IC 50 for some products in comparison with the standard drug, doxorubicin. On the other hand, antiviral activity of the synthesized products against H 5 N 1 showed moderate to weak activity compared to Zanamivir reference drug.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s00044-017-2083-7</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1054-2523
ispartof Medicinal chemistry research, 2018-02, Vol.27 (2), p.571-582
issn 1054-2523
1554-8120
language eng
recordid cdi_proquest_journals_2000307512
source SpringerLink (Online service)
subjects Adenocarcinoma
Anticancer properties
Antitumor activity
Antiviral activity
Biochemistry
Biomedical and Life Sciences
Biomedicine
Breast cancer
Cancer
Cell Biology
Cytotoxicity
Derivatives
Doxorubicin
Epithelial cells
Hepatocytes
Liver
Liver cancer
Original Research
Pharmacology/Toxicology
Pyrazoles
Quinazolinone
Synthesis
Toxicity
Tumor cell lines
Zanamivir
title New series of 4(3H)-quinazolinone derivatives: syntheses and evaluation of antitumor and antiviral activities
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T19%3A40%3A24IST&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=New%20series%20of%204(3H)-quinazolinone%20derivatives:%20syntheses%20and%20evaluation%20of%20antitumor%20and%20antiviral%20activities&rft.jtitle=Medicinal%20chemistry%20research&rft.au=Abbas,%20Samir%20Y.&rft.date=2018-02-01&rft.volume=27&rft.issue=2&rft.spage=571&rft.epage=582&rft.pages=571-582&rft.issn=1054-2523&rft.eissn=1554-8120&rft_id=info:doi/10.1007/s00044-017-2083-7&rft_dat=%3Cproquest_cross%3E2000307512%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=2000307512&rft_id=info:pmid/&rfr_iscdi=true