Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes
Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)...
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container_title | Journal of inorganic biochemistry |
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creator | Kozsup, Máté Zhou, XueQuan Farkas, Etelka Bényei, Attila Cs Bonnet, Sylvestre Patonay, Tamás Kónya, Krisztina Buglyó, Péter |
description | Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa) and flav = deprotonated form of differently substituted flavonols have been synthesized, characterized, and their cytotoxicity assayed under both normoxic and hypoxic conditions. Molecular structures of two free flavonols and seven complexes are also reported. In all the complexes the bioligands exhibited the expected (O,O) coordination mode and the complexes showed a slightly distorted octahedral geometry. Cyclic voltammetric studies revealed that both the substituents of the flavonoles and the type of 4N donor ligands had an impact on the reduction potential of the complex. The ones containing tren demonstrated significantly higher stability than the tpa analogues, making these former compounds promising candidates for the development of hypoxia-activated prodrug complexes. Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity.
Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. [Display omitted]
•Synthesis of [CoIII(4N)(flavonolato)]2+ type complexes with flavonoles as bioligands.•Chemical characterization of the novel complexes including X-ray studies.•Dependence of the redox behavior of the complexes on the tripodal tetramine (4N).•Biological assay of the complexes against A549 and A431 cancer cell lines. |
doi_str_mv | 10.1016/j.jinorgbio.2021.111382 |
format | Article |
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Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. [Display omitted]
•Synthesis of [CoIII(4N)(flavonolato)]2+ type complexes with flavonoles as bioligands.•Chemical characterization of the novel complexes including X-ray studies.•Dependence of the redox behavior of the complexes on the tripodal tetramine (4N).•Biological assay of the complexes against A549 and A431 cancer cell lines.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2021.111382</identifier><identifier>PMID: 33588278</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Anticancer ; Antineoplastic Agents - chemical synthesis ; Antineoplastic Agents - pharmacology ; Cell Hypoxia - physiology ; Cell Line, Tumor ; Cobalt - chemistry ; CoIII complexes ; Coordination Complexes - chemical synthesis ; Coordination Complexes - pharmacology ; Flavonoids - chemical synthesis ; Flavonoids - pharmacology ; Flavonoles ; Humans ; Hypoxia activation ; Ligands ; Molecular Structure ; Oxidation-Reduction ; Redox behavior ; Stereoisomerism ; X-ray structures</subject><ispartof>Journal of inorganic biochemistry, 2021-04, Vol.217, p.111382-111382, Article 111382</ispartof><rights>2021 The Authors</rights><rights>Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-942ad7928db1500bba13107b26ab75fde72f4a5e1665f1b4e64f59fbb6ff823a3</citedby><cites>FETCH-LOGICAL-c420t-942ad7928db1500bba13107b26ab75fde72f4a5e1665f1b4e64f59fbb6ff823a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinorgbio.2021.111382$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33588278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kozsup, Máté</creatorcontrib><creatorcontrib>Zhou, XueQuan</creatorcontrib><creatorcontrib>Farkas, Etelka</creatorcontrib><creatorcontrib>Bényei, Attila Cs</creatorcontrib><creatorcontrib>Bonnet, Sylvestre</creatorcontrib><creatorcontrib>Patonay, Tamás</creatorcontrib><creatorcontrib>Kónya, Krisztina</creatorcontrib><creatorcontrib>Buglyó, Péter</creatorcontrib><title>Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa) and flav = deprotonated form of differently substituted flavonols have been synthesized, characterized, and their cytotoxicity assayed under both normoxic and hypoxic conditions. Molecular structures of two free flavonols and seven complexes are also reported. In all the complexes the bioligands exhibited the expected (O,O) coordination mode and the complexes showed a slightly distorted octahedral geometry. Cyclic voltammetric studies revealed that both the substituents of the flavonoles and the type of 4N donor ligands had an impact on the reduction potential of the complex. The ones containing tren demonstrated significantly higher stability than the tpa analogues, making these former compounds promising candidates for the development of hypoxia-activated prodrug complexes. Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity.
Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. [Display omitted]
•Synthesis of [CoIII(4N)(flavonolato)]2+ type complexes with flavonoles as bioligands.•Chemical characterization of the novel complexes including X-ray studies.•Dependence of the redox behavior of the complexes on the tripodal tetramine (4N).•Biological assay of the complexes against A549 and A431 cancer cell lines.</description><subject>Anticancer</subject><subject>Antineoplastic Agents - chemical synthesis</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Cell Hypoxia - physiology</subject><subject>Cell Line, Tumor</subject><subject>Cobalt - chemistry</subject><subject>CoIII complexes</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - pharmacology</subject><subject>Flavonoids - chemical synthesis</subject><subject>Flavonoids - pharmacology</subject><subject>Flavonoles</subject><subject>Humans</subject><subject>Hypoxia activation</subject><subject>Ligands</subject><subject>Molecular Structure</subject><subject>Oxidation-Reduction</subject><subject>Redox behavior</subject><subject>Stereoisomerism</subject><subject>X-ray structures</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtOwzAQRS0EgvL4BcgSJFI8fiTpElU8KiGxANaW7YzBVRoX260oX09QgS2r2Zx7r-YQcgZ0DBSqq_l47vsQX40PY0YZjAGAN2yHjKCpecm5ELtkNJCspMDFATlMaU4plVLU--SAc9k0rG5G5OVp0-c3TD5dFvZNR20zRv-psw99ofu2sJsccvjw1udNkfKq9ZiK4IppOJ_NZhel6_Q69KHTORQ2LJYdfmA6JntOdwlPfu4Rebm9eZ7elw-Pd7Pp9UNpBaO5nAim23rCmtaApNQYDRxobVilTS1dizVzQkuEqpIOjMBKODlxxlTONYxrfkTOt73LGN5XmLJa-GSx63SPYZUUExMKgxGQA1pvURtDShGdWka_0HGjgKpvp2qu_pyqb6dq63RInv6MrMwC27_cr8QBuN4COLy69hhVsh57i62PaLNqg_935Avtl41Y</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Kozsup, Máté</creator><creator>Zhou, XueQuan</creator><creator>Farkas, Etelka</creator><creator>Bényei, Attila Cs</creator><creator>Bonnet, Sylvestre</creator><creator>Patonay, Tamás</creator><creator>Kónya, Krisztina</creator><creator>Buglyó, Péter</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope></search><sort><creationdate>202104</creationdate><title>Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes</title><author>Kozsup, Máté ; Zhou, XueQuan ; Farkas, Etelka ; Bényei, Attila Cs ; Bonnet, Sylvestre ; Patonay, Tamás ; Kónya, Krisztina ; Buglyó, Péter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-942ad7928db1500bba13107b26ab75fde72f4a5e1665f1b4e64f59fbb6ff823a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anticancer</topic><topic>Antineoplastic Agents - chemical synthesis</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Cell Hypoxia - physiology</topic><topic>Cell Line, Tumor</topic><topic>Cobalt - chemistry</topic><topic>CoIII complexes</topic><topic>Coordination Complexes - chemical synthesis</topic><topic>Coordination Complexes - pharmacology</topic><topic>Flavonoids - chemical synthesis</topic><topic>Flavonoids - pharmacology</topic><topic>Flavonoles</topic><topic>Humans</topic><topic>Hypoxia activation</topic><topic>Ligands</topic><topic>Molecular Structure</topic><topic>Oxidation-Reduction</topic><topic>Redox behavior</topic><topic>Stereoisomerism</topic><topic>X-ray structures</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kozsup, Máté</creatorcontrib><creatorcontrib>Zhou, XueQuan</creatorcontrib><creatorcontrib>Farkas, Etelka</creatorcontrib><creatorcontrib>Bényei, Attila Cs</creatorcontrib><creatorcontrib>Bonnet, Sylvestre</creatorcontrib><creatorcontrib>Patonay, Tamás</creatorcontrib><creatorcontrib>Kónya, Krisztina</creatorcontrib><creatorcontrib>Buglyó, Péter</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kozsup, Máté</au><au>Zhou, XueQuan</au><au>Farkas, Etelka</au><au>Bényei, Attila Cs</au><au>Bonnet, Sylvestre</au><au>Patonay, Tamás</au><au>Kónya, Krisztina</au><au>Buglyó, Péter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2021-04</date><risdate>2021</risdate><volume>217</volume><spage>111382</spage><epage>111382</epage><pages>111382-111382</pages><artnum>111382</artnum><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>Hypoxia activated Co(III) complexes as prodrugs may provide with a selective delivery of cytotoxic or antibacterial compounds. Whithin this field sixteen novel Co(III) ternary complexes with the general formula [Co(4N)(flav)](ClO4)2, where 4N = tris(2-aminoethyl)amine (tren) or tris(2-pyridylmethyl)amine (tpa) and flav = deprotonated form of differently substituted flavonols have been synthesized, characterized, and their cytotoxicity assayed under both normoxic and hypoxic conditions. Molecular structures of two free flavonols and seven complexes are also reported. In all the complexes the bioligands exhibited the expected (O,O) coordination mode and the complexes showed a slightly distorted octahedral geometry. Cyclic voltammetric studies revealed that both the substituents of the flavonoles and the type of 4N donor ligands had an impact on the reduction potential of the complex. The ones containing tren demonstrated significantly higher stability than the tpa analogues, making these former compounds promising candidates for the development of hypoxia-activated prodrug complexes. Tpa complexes showed higher activity against both selected human cancer cell lines (A549, A431) than their free ligand flavonols, indicating that the anticancer activity of the bioligand can be enhanced upon complexation. However, slight hypoxia-selectivity was found only for a tren complex (11) with moderate cytotoxicity.
Novel, multitargeted Co(III) complexes with flavonolate and ancillary 4N donor ligands have been synthesized, characterized and tested against selected human derived cancer cell lines under hypoxic and normoxic conditions. [Display omitted]
•Synthesis of [CoIII(4N)(flavonolato)]2+ type complexes with flavonoles as bioligands.•Chemical characterization of the novel complexes including X-ray studies.•Dependence of the redox behavior of the complexes on the tripodal tetramine (4N).•Biological assay of the complexes against A549 and A431 cancer cell lines.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>33588278</pmid><doi>10.1016/j.jinorgbio.2021.111382</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anticancer Antineoplastic Agents - chemical synthesis Antineoplastic Agents - pharmacology Cell Hypoxia - physiology Cell Line, Tumor Cobalt - chemistry CoIII complexes Coordination Complexes - chemical synthesis Coordination Complexes - pharmacology Flavonoids - chemical synthesis Flavonoids - pharmacology Flavonoles Humans Hypoxia activation Ligands Molecular Structure Oxidation-Reduction Redox behavior Stereoisomerism X-ray structures |
title | Synthesis, characterization and cytotoxicity studies of Co(III)-flavonolato complexes |
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