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Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts
A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes - and related quaternary ammonium salts - were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series and to be potent...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2021-11, Vol.26 (23), p.7132 |
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creator | Roayapalley, Praveen K Dimmock, Jonathan R Contreras, Lisett Balderrama, Karol S Aguilera, Renato J Sakagami, Hiroshi Amano, Shigeru Sharma, Rajendra K Das, Umashankar |
description | A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes
-
and related quaternary ammonium salts
-
were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series
and
to be potent cytotoxins with submicromolar CC
values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition,
-
are cytotoxic towards a number of leukemic and colon cancer cells.
,
lowered the mitochondrial membrane potential in CEM cells, and
induced transient G2/M accumulation in Ca9-22 cells. Five compounds, namely
,
and
, were identified as lead molecules that have drug-like properties. |
doi_str_mv | 10.3390/molecules26237132 |
format | article |
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-
and related quaternary ammonium salts
-
were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series
and
to be potent cytotoxins with submicromolar CC
values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition,
-
are cytotoxic towards a number of leukemic and colon cancer cells.
,
lowered the mitochondrial membrane potential in CEM cells, and
induced transient G2/M accumulation in Ca9-22 cells. Five compounds, namely
,
and
, were identified as lead molecules that have drug-like properties.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules26237132</identifier><identifier>PMID: 34885719</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Ammonium ; Ammonium salts ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - chemistry ; Antineoplastic Agents - pharmacology ; Apoptosis - drug effects ; Cancer ; Cell cycle ; Cell Line, Tumor ; Cell Proliferation - drug effects ; Colon ; Colon cancer ; Colonic Neoplasms - drug therapy ; Colorectal cancer ; conjugated unsaturated ketones ; Cytotoxicity ; Cytotoxins ; Fibroblasts ; Humans ; Laboratories ; Leukemia ; Membrane potential ; Mitochondria ; mitochondrial membrane potential ; Nitrogen ; Oximes ; Oximes - chemical synthesis ; Oximes - chemistry ; Oximes - pharmacology ; QSAR ; Quantitative Structure-Activity Relationship ; Quaternary Ammonium Compounds - chemical synthesis ; Quaternary Ammonium Compounds - chemistry ; Quaternary Ammonium Compounds - pharmacology ; Quaternary ammonium salts ; Salts ; Selectivity ; Toxicity ; Tumors</subject><ispartof>Molecules (Basel, Switzerland), 2021-11, Vol.26 (23), p.7132</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-1f836134c3f9532e5038900d9597cb6b46772d65154d8bcab4b27432b00c8ad03</citedby><cites>FETCH-LOGICAL-c493t-1f836134c3f9532e5038900d9597cb6b46772d65154d8bcab4b27432b00c8ad03</cites><orcidid>0000-0001-8001-2121 ; 0000-0003-3712-5790</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2608139128/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2608139128?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34885719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roayapalley, Praveen K</creatorcontrib><creatorcontrib>Dimmock, Jonathan R</creatorcontrib><creatorcontrib>Contreras, Lisett</creatorcontrib><creatorcontrib>Balderrama, Karol S</creatorcontrib><creatorcontrib>Aguilera, Renato J</creatorcontrib><creatorcontrib>Sakagami, Hiroshi</creatorcontrib><creatorcontrib>Amano, Shigeru</creatorcontrib><creatorcontrib>Sharma, Rajendra K</creatorcontrib><creatorcontrib>Das, Umashankar</creatorcontrib><title>Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes
-
and related quaternary ammonium salts
-
were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series
and
to be potent cytotoxins with submicromolar CC
values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition,
-
are cytotoxic towards a number of leukemic and colon cancer cells.
,
lowered the mitochondrial membrane potential in CEM cells, and
induced transient G2/M accumulation in Ca9-22 cells. Five compounds, namely
,
and
, were identified as lead molecules that have drug-like properties.</description><subject>Ammonium</subject><subject>Ammonium salts</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Cancer</subject><subject>Cell cycle</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation - drug effects</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colorectal cancer</subject><subject>conjugated unsaturated ketones</subject><subject>Cytotoxicity</subject><subject>Cytotoxins</subject><subject>Fibroblasts</subject><subject>Humans</subject><subject>Laboratories</subject><subject>Leukemia</subject><subject>Membrane potential</subject><subject>Mitochondria</subject><subject>mitochondrial membrane potential</subject><subject>Nitrogen</subject><subject>Oximes</subject><subject>Oximes - chemical synthesis</subject><subject>Oximes - chemistry</subject><subject>Oximes - pharmacology</subject><subject>QSAR</subject><subject>Quantitative Structure-Activity Relationship</subject><subject>Quaternary Ammonium Compounds - chemical synthesis</subject><subject>Quaternary Ammonium Compounds - chemistry</subject><subject>Quaternary Ammonium Compounds - pharmacology</subject><subject>Quaternary ammonium salts</subject><subject>Salts</subject><subject>Selectivity</subject><subject>Toxicity</subject><subject>Tumors</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkl1rFDEUhgdRbK3-AG8k4I1Co_maSXIj1PpVKBbd9UokZCaZbZaZZExmlh3Fv-RvNHXX0uLVOZyP5z0hb1E8xugFpRK97ENnm6mziVSEckzJneIQM4IgRUzevZEfFA9SWiNEMMPl_eKAMiFKjuVh8fuNTW7lj8Fi9uNlzhPQ3oDl1IcpwoXNAqPbWLAMW9e4cQahBR_DxnYAw68U_qTHJXzt0rPa-h9z54z19jlkMGwDxHBwg43OOB9-QXpVG2IY5u5bHti3grfgYut6u5P9bDs9WgM-TTlEr-MMTvo-eDf1YKG7MT0s7rW6S_bRPh4VX969XZ5-gOcX789OT85hwyQdIW4FrTBlDW1lSYktERUSISNLyZu6qlnFOTFViUtmRN3omtWEM0pqhBqhDaJHxdmOa4JeqyG6Pt-ignbqbyHEldJxdE1nlWASMS50aTBnrOXSIF5JibEmFUcVz6xXO9Yw1b01jfVj1N0t6O2Od5dqFTZKVKUkjGbA0z0ghu-TTaNa58_x-f2KVEhgKjEReQrvppoYUoq2vVbASF3ZRf1nl7zz5OZp1xv__EH_AA4Jvjc</recordid><startdate>20211125</startdate><enddate>20211125</enddate><creator>Roayapalley, Praveen K</creator><creator>Dimmock, Jonathan R</creator><creator>Contreras, Lisett</creator><creator>Balderrama, Karol S</creator><creator>Aguilera, Renato J</creator><creator>Sakagami, Hiroshi</creator><creator>Amano, Shigeru</creator><creator>Sharma, Rajendra K</creator><creator>Das, Umashankar</creator><general>MDPI AG</general><general>MDPI</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8001-2121</orcidid><orcidid>https://orcid.org/0000-0003-3712-5790</orcidid></search><sort><creationdate>20211125</creationdate><title>Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts</title><author>Roayapalley, Praveen K ; Dimmock, Jonathan R ; Contreras, Lisett ; Balderrama, Karol S ; Aguilera, Renato J ; Sakagami, Hiroshi ; Amano, Shigeru ; Sharma, Rajendra K ; Das, Umashankar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-1f836134c3f9532e5038900d9597cb6b46772d65154d8bcab4b27432b00c8ad03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ammonium</topic><topic>Ammonium salts</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis - drug effects</topic><topic>Cancer</topic><topic>Cell cycle</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation - drug effects</topic><topic>Colon</topic><topic>Colon cancer</topic><topic>Colonic Neoplasms - drug therapy</topic><topic>Colorectal cancer</topic><topic>conjugated unsaturated ketones</topic><topic>Cytotoxicity</topic><topic>Cytotoxins</topic><topic>Fibroblasts</topic><topic>Humans</topic><topic>Laboratories</topic><topic>Leukemia</topic><topic>Membrane potential</topic><topic>Mitochondria</topic><topic>mitochondrial membrane potential</topic><topic>Nitrogen</topic><topic>Oximes</topic><topic>Oximes - chemical synthesis</topic><topic>Oximes - chemistry</topic><topic>Oximes - pharmacology</topic><topic>QSAR</topic><topic>Quantitative Structure-Activity Relationship</topic><topic>Quaternary Ammonium Compounds - chemical synthesis</topic><topic>Quaternary Ammonium Compounds - chemistry</topic><topic>Quaternary Ammonium Compounds - pharmacology</topic><topic>Quaternary ammonium salts</topic><topic>Salts</topic><topic>Selectivity</topic><topic>Toxicity</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roayapalley, Praveen K</creatorcontrib><creatorcontrib>Dimmock, Jonathan R</creatorcontrib><creatorcontrib>Contreras, Lisett</creatorcontrib><creatorcontrib>Balderrama, Karol S</creatorcontrib><creatorcontrib>Aguilera, Renato J</creatorcontrib><creatorcontrib>Sakagami, Hiroshi</creatorcontrib><creatorcontrib>Amano, Shigeru</creatorcontrib><creatorcontrib>Sharma, Rajendra K</creatorcontrib><creatorcontrib>Das, Umashankar</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roayapalley, Praveen K</au><au>Dimmock, Jonathan R</au><au>Contreras, Lisett</au><au>Balderrama, Karol S</au><au>Aguilera, Renato J</au><au>Sakagami, Hiroshi</au><au>Amano, Shigeru</au><au>Sharma, Rajendra K</au><au>Das, Umashankar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2021-11-25</date><risdate>2021</risdate><volume>26</volume><issue>23</issue><spage>7132</spage><pages>7132-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>A novel series of 1-[3-{3,5-bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone oximes
-
and related quaternary ammonium salts
-
were prepared as candidate antineoplastic agents. Evaluation against neoplastic Ca9-22, HSC-2 and HSC-4 cells revealed the compounds in series
and
to be potent cytotoxins with submicromolar CC
values in virtually all cases. In contrast, the compounds were less cytocidal towards HGF, HPLF and HPC non-malignant cells revealing their tumour-selective toxicity. Quantitative structure-activity relationships revealed that, in general, both cytotoxic potency and selectivity index figures increased as the magnitude of the Hammett sigma values rose. In addition,
-
are cytotoxic towards a number of leukemic and colon cancer cells.
,
lowered the mitochondrial membrane potential in CEM cells, and
induced transient G2/M accumulation in Ca9-22 cells. Five compounds, namely
,
and
, were identified as lead molecules that have drug-like properties.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>34885719</pmid><doi>10.3390/molecules26237132</doi><orcidid>https://orcid.org/0000-0001-8001-2121</orcidid><orcidid>https://orcid.org/0000-0003-3712-5790</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Publicly Available Content (ProQuest); PubMed Central |
subjects | Ammonium Ammonium salts Antineoplastic Agents - chemical synthesis Antineoplastic Agents - chemistry Antineoplastic Agents - pharmacology Apoptosis - drug effects Cancer Cell cycle Cell Line, Tumor Cell Proliferation - drug effects Colon Colon cancer Colonic Neoplasms - drug therapy Colorectal cancer conjugated unsaturated ketones Cytotoxicity Cytotoxins Fibroblasts Humans Laboratories Leukemia Membrane potential Mitochondria mitochondrial membrane potential Nitrogen Oximes Oximes - chemical synthesis Oximes - chemistry Oximes - pharmacology QSAR Quantitative Structure-Activity Relationship Quaternary Ammonium Compounds - chemical synthesis Quaternary Ammonium Compounds - chemistry Quaternary Ammonium Compounds - pharmacology Quaternary ammonium salts Salts Selectivity Toxicity Tumors |
title | Design, Synthesis and Tumour-Selective Toxicity of Novel 1-[3-{3,5-Bis(benzylidene)-4-oxo-1-piperidino}-3-oxopropyl]-4-piperidone Oximes and Related Quaternary Ammonium Salts |
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