Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide
Sulphonamides and carboxamides have shown large number of pharmacological properties against different types of diseases among which is malaria. Twenty four new carboxamide derivatives bearing benzenesulphonamoyl alkanamides were synthesized and investigated for their in silico and in vitro antimala...
Gespeichert in:
Veröffentlicht in: | European journal of medicinal chemistry 2017-07, Vol.135, p.349-369 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 369 |
---|---|
container_issue | |
container_start_page | 349 |
container_title | European journal of medicinal chemistry |
container_volume | 135 |
creator | Ugwu, D.I. Okoro, U.C. Ukoha, P.O. Okafor, S. Ibezim, A. Kumar, N.M. |
description | Sulphonamides and carboxamides have shown large number of pharmacological properties against different types of diseases among which is malaria. Twenty four new carboxamide derivatives bearing benzenesulphonamoyl alkanamides were synthesized and investigated for their in silico and in vitro antimalarial and antioxidant properties. The substituted benzenesulphonyl chlorides (1a-c) were treated with various amino acids (2a-h) to obtain the benzenesulphonamoyl alkanamides (3a-x) which were subsequently treated with benzoyl chloride to obtain the N-benzoylated derivatives (5a-f, i-n and q-v). Further reactions of the N-benzoylated derivatives or proline derivatives with 4-aminoacetophenone (6) using boric acid as a catalyst gave the sulphonamide carboxamide derivatives (7a-x) in excellent yields. The in vitro antimalarial studies showed that all synthesized compounds had antimalarial property. Compound 7k, 7c, 7l, 7s, and 7j had mean MIC value of 0.02, 0.03, 0.05, 0.06 and 0.08 μM respectively comparable with chloroquine 0.06 μM. Compound 7c was the most potent antioxidant agent with IC50 value of 0.045 mM comparable with 0.34 mM for ascorbic acid. In addition to the successful synthesis of the target molecules using boric acid catalysis, the compounds were found to have antimalarial and antioxidant activities comparable with known antimalarial and antioxidant drugs. The class of compounds reported herein have the potential of reducing oxidative stress arising from malaria parasite and chemotherapeutic agent used in the treatment of malaria.
[Display omitted]
•The development of multidrug resistant Plasmodium specie threatens the treatment of malaria.•Carboxamides and sulphonamides have been reported to possess fascinating antimalarial activities.•Malaria treatment often generates free radical species because most antimalarial agents are pro-oxidant.•Antimalarial agents with accompanied antioxidant activities will eradicate complications in malaria chemotherapy. |
doi_str_mv | 10.1016/j.ejmech.2017.04.029 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1894519285</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0223523417302866</els_id><sourcerecordid>1894519285</sourcerecordid><originalsourceid>FETCH-LOGICAL-c428t-3f97082e612cde5d71c84ccf0d2fc4d1053a0c39e6db0954be0309fa8a3294fe3</originalsourceid><addsrcrecordid>eNp9kM1u1DAQgC0EotvCGyCUI4cmjH-STS5IqAKKVIkDcLac8YT1ktiL7RSKxLvwLDwZLls4chrN-JsZz8fYEw4NB9493ze0Xwh3jQC-bUA1IIZ7bMO3XV9L0ar7bANCyLoVUp2w05T2ANB2AA_ZiehVB5LDhv14f-PzjpJL5xXuTDSYKbrvJrvgz6slzITrbGJlA352_lNlvK2c__Xz2uUYSpbdYsq7M3N1iOFAMTtKVZgqT18rNHEM38zibKmNVLAyIa3zYRf8n-oj9mAyc6LHd_GMfXz96sPFZX317s3bi5dXNSrR51pOwxZ6QR0XaKm1W469QpzAigmV5dBKAygH6uwIQ6tGAgnDZHojxaAmkmfs2XFu-eOXlVLWi0tI82w8hTVp3g-q5YPo24KqI4oxpBRp0odYbow3moO-Fa_3-ihe34rXoHQRX9qe3m1Yx4Xsv6a_pgvw4ghQufPaUdQJHXkk6yJh1ja4_2_4DYMamjw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1894519285</pqid></control><display><type>article</type><title>Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Ugwu, D.I. ; Okoro, U.C. ; Ukoha, P.O. ; Okafor, S. ; Ibezim, A. ; Kumar, N.M.</creator><creatorcontrib>Ugwu, D.I. ; Okoro, U.C. ; Ukoha, P.O. ; Okafor, S. ; Ibezim, A. ; Kumar, N.M.</creatorcontrib><description>Sulphonamides and carboxamides have shown large number of pharmacological properties against different types of diseases among which is malaria. Twenty four new carboxamide derivatives bearing benzenesulphonamoyl alkanamides were synthesized and investigated for their in silico and in vitro antimalarial and antioxidant properties. The substituted benzenesulphonyl chlorides (1a-c) were treated with various amino acids (2a-h) to obtain the benzenesulphonamoyl alkanamides (3a-x) which were subsequently treated with benzoyl chloride to obtain the N-benzoylated derivatives (5a-f, i-n and q-v). Further reactions of the N-benzoylated derivatives or proline derivatives with 4-aminoacetophenone (6) using boric acid as a catalyst gave the sulphonamide carboxamide derivatives (7a-x) in excellent yields. The in vitro antimalarial studies showed that all synthesized compounds had antimalarial property. Compound 7k, 7c, 7l, 7s, and 7j had mean MIC value of 0.02, 0.03, 0.05, 0.06 and 0.08 μM respectively comparable with chloroquine 0.06 μM. Compound 7c was the most potent antioxidant agent with IC50 value of 0.045 mM comparable with 0.34 mM for ascorbic acid. In addition to the successful synthesis of the target molecules using boric acid catalysis, the compounds were found to have antimalarial and antioxidant activities comparable with known antimalarial and antioxidant drugs. The class of compounds reported herein have the potential of reducing oxidative stress arising from malaria parasite and chemotherapeutic agent used in the treatment of malaria.
[Display omitted]
•The development of multidrug resistant Plasmodium specie threatens the treatment of malaria.•Carboxamides and sulphonamides have been reported to possess fascinating antimalarial activities.•Malaria treatment often generates free radical species because most antimalarial agents are pro-oxidant.•Antimalarial agents with accompanied antioxidant activities will eradicate complications in malaria chemotherapy.</description><identifier>ISSN: 0223-5234</identifier><identifier>EISSN: 1768-3254</identifier><identifier>DOI: 10.1016/j.ejmech.2017.04.029</identifier><identifier>PMID: 28460310</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Antimalarial ; Antimalarials - chemical synthesis ; Antimalarials - chemistry ; Antimalarials - pharmacology ; Antioxidant ; Carboxamides ; Dose-Response Relationship, Drug ; Malaria - drug therapy ; Molecular Docking Simulation ; Molecular Structure ; Parasitic Sensitivity Tests ; Plasmepsin II ; Plasmodium falciparum - drug effects ; SAR ; Structure-Activity Relationship ; Sulfonamides - chemistry ; Sulfonamides - pharmacology ; Sulphonamides</subject><ispartof>European journal of medicinal chemistry, 2017-07, Vol.135, p.349-369</ispartof><rights>2017 Elsevier Masson SAS</rights><rights>Copyright © 2017 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-3f97082e612cde5d71c84ccf0d2fc4d1053a0c39e6db0954be0309fa8a3294fe3</citedby><cites>FETCH-LOGICAL-c428t-3f97082e612cde5d71c84ccf0d2fc4d1053a0c39e6db0954be0309fa8a3294fe3</cites><orcidid>0000-0002-2370-6191</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejmech.2017.04.029$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28460310$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ugwu, D.I.</creatorcontrib><creatorcontrib>Okoro, U.C.</creatorcontrib><creatorcontrib>Ukoha, P.O.</creatorcontrib><creatorcontrib>Okafor, S.</creatorcontrib><creatorcontrib>Ibezim, A.</creatorcontrib><creatorcontrib>Kumar, N.M.</creatorcontrib><title>Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide</title><title>European journal of medicinal chemistry</title><addtitle>Eur J Med Chem</addtitle><description>Sulphonamides and carboxamides have shown large number of pharmacological properties against different types of diseases among which is malaria. Twenty four new carboxamide derivatives bearing benzenesulphonamoyl alkanamides were synthesized and investigated for their in silico and in vitro antimalarial and antioxidant properties. The substituted benzenesulphonyl chlorides (1a-c) were treated with various amino acids (2a-h) to obtain the benzenesulphonamoyl alkanamides (3a-x) which were subsequently treated with benzoyl chloride to obtain the N-benzoylated derivatives (5a-f, i-n and q-v). Further reactions of the N-benzoylated derivatives or proline derivatives with 4-aminoacetophenone (6) using boric acid as a catalyst gave the sulphonamide carboxamide derivatives (7a-x) in excellent yields. The in vitro antimalarial studies showed that all synthesized compounds had antimalarial property. Compound 7k, 7c, 7l, 7s, and 7j had mean MIC value of 0.02, 0.03, 0.05, 0.06 and 0.08 μM respectively comparable with chloroquine 0.06 μM. Compound 7c was the most potent antioxidant agent with IC50 value of 0.045 mM comparable with 0.34 mM for ascorbic acid. In addition to the successful synthesis of the target molecules using boric acid catalysis, the compounds were found to have antimalarial and antioxidant activities comparable with known antimalarial and antioxidant drugs. The class of compounds reported herein have the potential of reducing oxidative stress arising from malaria parasite and chemotherapeutic agent used in the treatment of malaria.
[Display omitted]
•The development of multidrug resistant Plasmodium specie threatens the treatment of malaria.•Carboxamides and sulphonamides have been reported to possess fascinating antimalarial activities.•Malaria treatment often generates free radical species because most antimalarial agents are pro-oxidant.•Antimalarial agents with accompanied antioxidant activities will eradicate complications in malaria chemotherapy.</description><subject>Antimalarial</subject><subject>Antimalarials - chemical synthesis</subject><subject>Antimalarials - chemistry</subject><subject>Antimalarials - pharmacology</subject><subject>Antioxidant</subject><subject>Carboxamides</subject><subject>Dose-Response Relationship, Drug</subject><subject>Malaria - drug therapy</subject><subject>Molecular Docking Simulation</subject><subject>Molecular Structure</subject><subject>Parasitic Sensitivity Tests</subject><subject>Plasmepsin II</subject><subject>Plasmodium falciparum - drug effects</subject><subject>SAR</subject><subject>Structure-Activity Relationship</subject><subject>Sulfonamides - chemistry</subject><subject>Sulfonamides - pharmacology</subject><subject>Sulphonamides</subject><issn>0223-5234</issn><issn>1768-3254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1u1DAQgC0EotvCGyCUI4cmjH-STS5IqAKKVIkDcLac8YT1ktiL7RSKxLvwLDwZLls4chrN-JsZz8fYEw4NB9493ze0Xwh3jQC-bUA1IIZ7bMO3XV9L0ar7bANCyLoVUp2w05T2ANB2AA_ZiehVB5LDhv14f-PzjpJL5xXuTDSYKbrvJrvgz6slzITrbGJlA352_lNlvK2c__Xz2uUYSpbdYsq7M3N1iOFAMTtKVZgqT18rNHEM38zibKmNVLAyIa3zYRf8n-oj9mAyc6LHd_GMfXz96sPFZX317s3bi5dXNSrR51pOwxZ6QR0XaKm1W469QpzAigmV5dBKAygH6uwIQ6tGAgnDZHojxaAmkmfs2XFu-eOXlVLWi0tI82w8hTVp3g-q5YPo24KqI4oxpBRp0odYbow3moO-Fa_3-ihe34rXoHQRX9qe3m1Yx4Xsv6a_pgvw4ghQufPaUdQJHXkk6yJh1ja4_2_4DYMamjw</recordid><startdate>20170728</startdate><enddate>20170728</enddate><creator>Ugwu, D.I.</creator><creator>Okoro, U.C.</creator><creator>Ukoha, P.O.</creator><creator>Okafor, S.</creator><creator>Ibezim, A.</creator><creator>Kumar, N.M.</creator><general>Elsevier Masson SAS</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><orcidid>https://orcid.org/0000-0002-2370-6191</orcidid></search><sort><creationdate>20170728</creationdate><title>Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide</title><author>Ugwu, D.I. ; Okoro, U.C. ; Ukoha, P.O. ; Okafor, S. ; Ibezim, A. ; Kumar, N.M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-3f97082e612cde5d71c84ccf0d2fc4d1053a0c39e6db0954be0309fa8a3294fe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antimalarial</topic><topic>Antimalarials - chemical synthesis</topic><topic>Antimalarials - chemistry</topic><topic>Antimalarials - pharmacology</topic><topic>Antioxidant</topic><topic>Carboxamides</topic><topic>Dose-Response Relationship, Drug</topic><topic>Malaria - drug therapy</topic><topic>Molecular Docking Simulation</topic><topic>Molecular Structure</topic><topic>Parasitic Sensitivity Tests</topic><topic>Plasmepsin II</topic><topic>Plasmodium falciparum - drug effects</topic><topic>SAR</topic><topic>Structure-Activity Relationship</topic><topic>Sulfonamides - chemistry</topic><topic>Sulfonamides - pharmacology</topic><topic>Sulphonamides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ugwu, D.I.</creatorcontrib><creatorcontrib>Okoro, U.C.</creatorcontrib><creatorcontrib>Ukoha, P.O.</creatorcontrib><creatorcontrib>Okafor, S.</creatorcontrib><creatorcontrib>Ibezim, A.</creatorcontrib><creatorcontrib>Kumar, N.M.</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>European journal of medicinal chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ugwu, D.I.</au><au>Okoro, U.C.</au><au>Ukoha, P.O.</au><au>Okafor, S.</au><au>Ibezim, A.</au><au>Kumar, N.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide</atitle><jtitle>European journal of medicinal chemistry</jtitle><addtitle>Eur J Med Chem</addtitle><date>2017-07-28</date><risdate>2017</risdate><volume>135</volume><spage>349</spage><epage>369</epage><pages>349-369</pages><issn>0223-5234</issn><eissn>1768-3254</eissn><abstract>Sulphonamides and carboxamides have shown large number of pharmacological properties against different types of diseases among which is malaria. Twenty four new carboxamide derivatives bearing benzenesulphonamoyl alkanamides were synthesized and investigated for their in silico and in vitro antimalarial and antioxidant properties. The substituted benzenesulphonyl chlorides (1a-c) were treated with various amino acids (2a-h) to obtain the benzenesulphonamoyl alkanamides (3a-x) which were subsequently treated with benzoyl chloride to obtain the N-benzoylated derivatives (5a-f, i-n and q-v). Further reactions of the N-benzoylated derivatives or proline derivatives with 4-aminoacetophenone (6) using boric acid as a catalyst gave the sulphonamide carboxamide derivatives (7a-x) in excellent yields. The in vitro antimalarial studies showed that all synthesized compounds had antimalarial property. Compound 7k, 7c, 7l, 7s, and 7j had mean MIC value of 0.02, 0.03, 0.05, 0.06 and 0.08 μM respectively comparable with chloroquine 0.06 μM. Compound 7c was the most potent antioxidant agent with IC50 value of 0.045 mM comparable with 0.34 mM for ascorbic acid. In addition to the successful synthesis of the target molecules using boric acid catalysis, the compounds were found to have antimalarial and antioxidant activities comparable with known antimalarial and antioxidant drugs. The class of compounds reported herein have the potential of reducing oxidative stress arising from malaria parasite and chemotherapeutic agent used in the treatment of malaria.
[Display omitted]
•The development of multidrug resistant Plasmodium specie threatens the treatment of malaria.•Carboxamides and sulphonamides have been reported to possess fascinating antimalarial activities.•Malaria treatment often generates free radical species because most antimalarial agents are pro-oxidant.•Antimalarial agents with accompanied antioxidant activities will eradicate complications in malaria chemotherapy.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>28460310</pmid><doi>10.1016/j.ejmech.2017.04.029</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-2370-6191</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0223-5234 |
ispartof | European journal of medicinal chemistry, 2017-07, Vol.135, p.349-369 |
issn | 0223-5234 1768-3254 |
language | eng |
recordid | cdi_proquest_miscellaneous_1894519285 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Antimalarial Antimalarials - chemical synthesis Antimalarials - chemistry Antimalarials - pharmacology Antioxidant Carboxamides Dose-Response Relationship, Drug Malaria - drug therapy Molecular Docking Simulation Molecular Structure Parasitic Sensitivity Tests Plasmepsin II Plasmodium falciparum - drug effects SAR Structure-Activity Relationship Sulfonamides - chemistry Sulfonamides - pharmacology Sulphonamides |
title | Synthesis, characterization, molecular docking and in vitro antimalarial properties of new carboxamides bearing sulphonamide |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T04%3A13%3A05IST&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,%20characterization,%20molecular%20docking%20and%20in%C2%A0vitro%20antimalarial%20properties%20of%20new%20carboxamides%20bearing%20sulphonamide&rft.jtitle=European%20journal%20of%20medicinal%20chemistry&rft.au=Ugwu,%20D.I.&rft.date=2017-07-28&rft.volume=135&rft.spage=349&rft.epage=369&rft.pages=349-369&rft.issn=0223-5234&rft.eissn=1768-3254&rft_id=info:doi/10.1016/j.ejmech.2017.04.029&rft_dat=%3Cproquest_cross%3E1894519285%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=1894519285&rft_id=info:pmid/28460310&rft_els_id=S0223523417302866&rfr_iscdi=true |