Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes
Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore,...
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creator | Silva, Giovani Lindolfo Dias, Júlia Scaff Moreira Silva, Henrique Vieira Reis Teixeira, Jessica Da Silva De Souza, Ijaiel Rian Brito Guimarães, Elisalva Teixeira de Magalhães Moreira, Diogo Rodrigo Soares, Milena Botelho Pereira Barbosa, Marília Imaculada Frazão Doriguetto, Antônio Carlos |
description | Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity.
Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted]
•New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent. |
doi_str_mv | 10.1016/j.jinorgbio.2020.111002 |
format | Article |
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Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted]
•New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2020.111002</identifier><identifier>PMID: 32007697</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Antiprotozoal Agents - chemical synthesis ; Antiprotozoal Agents - chemistry ; Antiprotozoal Agents - pharmacology ; Cell Line ; Coordination Complexes - chemical synthesis ; Coordination Complexes - chemistry ; Coordination Complexes - pharmacology ; Copper - chemistry ; Copper - pharmacology ; Crystallography, X-Ray ; L. amazonensis ; Leishmania - growth & development ; Leishmaniasis - drug therapy ; Leishmaniasis - metabolism ; Leishmaniasis - pathology ; Leishmanicidal activity ; Mice ; Molecular Structure ; Platinum - chemistry ; Platinum - pharmacology ; Ru(III), Pt(II), Cu(II) complexes ; Rubidium - chemistry ; Rubidium - pharmacology ; Selectivity ; Trimethoprim ; Trimethoprim - chemistry ; Trimethoprim - pharmacology</subject><ispartof>Journal of inorganic biochemistry, 2020-04, Vol.205, p.111002-111002, Article 111002</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-991f77b862373bb44d99c3fc8bc409b110625a27d4179974264ab61c6899e6e93</citedby><cites>FETCH-LOGICAL-c371t-991f77b862373bb44d99c3fc8bc409b110625a27d4179974264ab61c6899e6e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0162013419307949$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32007697$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Silva, Giovani Lindolfo</creatorcontrib><creatorcontrib>Dias, Júlia Scaff Moreira</creatorcontrib><creatorcontrib>Silva, Henrique Vieira Reis</creatorcontrib><creatorcontrib>Teixeira, Jessica Da Silva</creatorcontrib><creatorcontrib>De Souza, Ijaiel Rian Brito</creatorcontrib><creatorcontrib>Guimarães, Elisalva Teixeira</creatorcontrib><creatorcontrib>de Magalhães Moreira, Diogo Rodrigo</creatorcontrib><creatorcontrib>Soares, Milena Botelho Pereira</creatorcontrib><creatorcontrib>Barbosa, Marília Imaculada Frazão</creatorcontrib><creatorcontrib>Doriguetto, Antônio Carlos</creatorcontrib><title>Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity.
Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted]
•New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</description><subject>Animals</subject><subject>Antiprotozoal Agents - chemical synthesis</subject><subject>Antiprotozoal Agents - chemistry</subject><subject>Antiprotozoal Agents - pharmacology</subject><subject>Cell Line</subject><subject>Coordination Complexes - chemical synthesis</subject><subject>Coordination Complexes - chemistry</subject><subject>Coordination Complexes - pharmacology</subject><subject>Copper - chemistry</subject><subject>Copper - pharmacology</subject><subject>Crystallography, X-Ray</subject><subject>L. amazonensis</subject><subject>Leishmania - growth & development</subject><subject>Leishmaniasis - drug therapy</subject><subject>Leishmaniasis - metabolism</subject><subject>Leishmaniasis - pathology</subject><subject>Leishmanicidal activity</subject><subject>Mice</subject><subject>Molecular Structure</subject><subject>Platinum - chemistry</subject><subject>Platinum - pharmacology</subject><subject>Ru(III), Pt(II), Cu(II) complexes</subject><subject>Rubidium - chemistry</subject><subject>Rubidium - pharmacology</subject><subject>Selectivity</subject><subject>Trimethoprim</subject><subject>Trimethoprim - chemistry</subject><subject>Trimethoprim - pharmacology</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PGzEQxS1EVQLtV6A-gsQG_4sdH1FUIBJSK6Bny-udbRztroPthebb4xDg2tOMZn5vRu8h9IOSKSVUXq6naz-E-Lf2YcoIK1NKCWEHaELnilecC3GIJoVkFaFcHKHjlNaEkNlMqK_oiDNClNRqgl4etkNeQfLpAru4Tdl2OOU4ujxGwHZocAc-rXo7eOebsrQu-2eftzi0eIAXnKPvIa_CplR8P54tl8vzC7zYNedv-t_5rS1QUbvQbzr4B-kb-tLaLsH393qC_lz_fFzcVne_bpaLq7vKcUVzpTVtlarnknHF61qIRmvHWzevnSC6LqYlm1mmGkGV1kowKWwtqZNzrUGC5ifobH93E8PTCCmb3icHXWcHCGMyjM8I55pIWVC1R10MKUVozc6TjVtDidmlbtbmM3WzS93sUy_K0_cnY91D86n7iLkAV3sAitVnD9Ek52Fw0PgILpsm-P8-eQV_A5Zo</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Silva, Giovani Lindolfo</creator><creator>Dias, Júlia Scaff Moreira</creator><creator>Silva, Henrique Vieira Reis</creator><creator>Teixeira, Jessica Da Silva</creator><creator>De Souza, Ijaiel Rian Brito</creator><creator>Guimarães, Elisalva Teixeira</creator><creator>de Magalhães Moreira, Diogo Rodrigo</creator><creator>Soares, Milena Botelho Pereira</creator><creator>Barbosa, Marília Imaculada Frazão</creator><creator>Doriguetto, Antônio Carlos</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>202004</creationdate><title>Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes</title><author>Silva, Giovani Lindolfo ; Dias, Júlia Scaff Moreira ; Silva, Henrique Vieira Reis ; Teixeira, Jessica Da Silva ; De Souza, Ijaiel Rian Brito ; Guimarães, Elisalva Teixeira ; de Magalhães Moreira, Diogo Rodrigo ; Soares, Milena Botelho Pereira ; Barbosa, Marília Imaculada Frazão ; Doriguetto, Antônio Carlos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-991f77b862373bb44d99c3fc8bc409b110625a27d4179974264ab61c6899e6e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antiprotozoal Agents - chemical synthesis</topic><topic>Antiprotozoal Agents - chemistry</topic><topic>Antiprotozoal Agents - pharmacology</topic><topic>Cell Line</topic><topic>Coordination Complexes - chemical synthesis</topic><topic>Coordination Complexes - chemistry</topic><topic>Coordination Complexes - pharmacology</topic><topic>Copper - chemistry</topic><topic>Copper - pharmacology</topic><topic>Crystallography, X-Ray</topic><topic>L. amazonensis</topic><topic>Leishmania - growth & development</topic><topic>Leishmaniasis - drug therapy</topic><topic>Leishmaniasis - metabolism</topic><topic>Leishmaniasis - pathology</topic><topic>Leishmanicidal activity</topic><topic>Mice</topic><topic>Molecular Structure</topic><topic>Platinum - chemistry</topic><topic>Platinum - pharmacology</topic><topic>Ru(III), Pt(II), Cu(II) complexes</topic><topic>Rubidium - chemistry</topic><topic>Rubidium - pharmacology</topic><topic>Selectivity</topic><topic>Trimethoprim</topic><topic>Trimethoprim - chemistry</topic><topic>Trimethoprim - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silva, Giovani Lindolfo</creatorcontrib><creatorcontrib>Dias, Júlia Scaff Moreira</creatorcontrib><creatorcontrib>Silva, Henrique Vieira Reis</creatorcontrib><creatorcontrib>Teixeira, Jessica Da Silva</creatorcontrib><creatorcontrib>De Souza, Ijaiel Rian Brito</creatorcontrib><creatorcontrib>Guimarães, Elisalva Teixeira</creatorcontrib><creatorcontrib>de Magalhães Moreira, Diogo Rodrigo</creatorcontrib><creatorcontrib>Soares, Milena Botelho Pereira</creatorcontrib><creatorcontrib>Barbosa, Marília Imaculada Frazão</creatorcontrib><creatorcontrib>Doriguetto, Antônio Carlos</creatorcontrib><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>Silva, Giovani Lindolfo</au><au>Dias, Júlia Scaff Moreira</au><au>Silva, Henrique Vieira Reis</au><au>Teixeira, Jessica Da Silva</au><au>De Souza, Ijaiel Rian Brito</au><au>Guimarães, Elisalva Teixeira</au><au>de Magalhães Moreira, Diogo Rodrigo</au><au>Soares, Milena Botelho Pereira</au><au>Barbosa, Marília Imaculada Frazão</au><au>Doriguetto, Antônio Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2020-04</date><risdate>2020</risdate><volume>205</volume><spage>111002</spage><epage>111002</epage><pages>111002-111002</pages><artnum>111002</artnum><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>Leishmaniasis is a parasitic disease caused by protozoa of the genus Leishmania, which has very limited treatment options and affects poor and underdeveloped populations. The current treatment is plagued by many complications, such as high toxicity, high cost and resistance to parasites; therefore, novel therapeutic agents are urgently needed. Herein, the synthesis, characterization and in vitro leishmanicidal potential of new complexes with the general formula [RuCl3(TMP)(dppb)] (1), [PtCl(TMP)(PPh3)2]PF6 (2) and [Cu(CH3COO)2(TMP)2]·DMF (3) (dppb = 1,4-bis(diphenylphosphino)butane, PPH3 = triphenylphosphine and TMP = trimethoprim) were evaluated. The complexes were characterized by infrared, UV–vis, cyclic voltammetry, molar conductance measurements, elemental analysis and NMR experiments. Also, the geometry of (2) and (3) were determined by single crystal X-ray diffraction. Despite being less potent against promastigote L. amazonensis proliferation than amphotericin B reference drug (IC50 = 0.09 ± 0.02 μM), complex (2) (IC50 = 3.6 ± 1.5 μM) was several times less cytotoxic (CC50 = 17.8 μM, SI = 4.9) in comparison with amphotericin B (CC50 = 3.3 μM, SI = 36.6) and gentian violet control (CC50 = 0.8 μM). Additionally, complex (2) inhibited J774 macrophage infection and amastigote number by macrophages (IC50 = 6.6 and SI = 2.7). Outstandingly, complex (2) was shown to be a promising candidate for a new leishmanicidal therapeutic agent, considering its biological power combined with low toxicity.
Trimethoprim complexes with ruthenium(III), platinum(II) and cooper(II) were synthesized and characterized and their leishmanicidal activity evaluated. The platinum complex exhibited promising leishmanicidal activity and low toxicity. [Display omitted]
•New trimethoprim Ru(III), Cu(II) and Pt(II) complexes are reported.•The crystal structure of the Cu(II) and Pt(II) complexes are determined.•The Pt(II) complex is a promising candidate for a leishmanicidal therapeutic agent.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32007697</pmid><doi>10.1016/j.jinorgbio.2020.111002</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Antiprotozoal Agents - chemical synthesis Antiprotozoal Agents - chemistry Antiprotozoal Agents - pharmacology Cell Line Coordination Complexes - chemical synthesis Coordination Complexes - chemistry Coordination Complexes - pharmacology Copper - chemistry Copper - pharmacology Crystallography, X-Ray L. amazonensis Leishmania - growth & development Leishmaniasis - drug therapy Leishmaniasis - metabolism Leishmaniasis - pathology Leishmanicidal activity Mice Molecular Structure Platinum - chemistry Platinum - pharmacology Ru(III), Pt(II), Cu(II) complexes Rubidium - chemistry Rubidium - pharmacology Selectivity Trimethoprim Trimethoprim - chemistry Trimethoprim - pharmacology |
title | Synthesis, crystal structure and leishmanicidal activity of new trimethoprim Ru(III), Cu(II) and Pt(II) metal complexes |
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