Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane

A series of new bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl)methane 3(a–d)/5(a–f) were synthesized from bis‐(4‐aminophenyl)methane (1) using various pharmacologically active sulfonyl chlorides 2(a–d) and carbonochloridates 4(a–f) in high yields. The structures of all the newly synthe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the Chinese Chemical Society (Taipei) 2020-07, Vol.67 (7), p.1289-1295
Hauptverfasser: Nagalakshmamma, Vadabingi, Varalakshmi, Mavallur, Umapriya, Kollu, Venkataswamy, Mallepogu, Venkataramaiah, Chintha, Thyaga Raju, Kedam, Chalapathi, Ponne Venkata, NagaRaju, Chamarthi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1295
container_issue 7
container_start_page 1289
container_title Journal of the Chinese Chemical Society (Taipei)
container_volume 67
creator Nagalakshmamma, Vadabingi
Varalakshmi, Mavallur
Umapriya, Kollu
Venkataswamy, Mallepogu
Venkataramaiah, Chintha
Thyaga Raju, Kedam
Chalapathi, Ponne Venkata
NagaRaju, Chamarthi
description A series of new bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl)methane 3(a–d)/5(a–f) were synthesized from bis‐(4‐aminophenyl)methane (1) using various pharmacologically active sulfonyl chlorides 2(a–d) and carbonochloridates 4(a–f) in high yields. The structures of all the newly synthesized compounds were characterized by the Infrared spectroscopy, NMR (1H and 13C), mass, and elemental analyses. Further, all the synthesized compounds were tested for the antioxidant activity by using 2, 2‐diphenyl‐1‐picrylhydrazyl, NO, and H2O2 scavenging methods and antimicrobial activity. Most of the compounds exhibited good antioxidant and antimicrobial activities.
doi_str_mv 10.1002/jccs.201900434
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2422435739</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2422435739</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3544-1ce738f7d3110cc7e3bf151acc9db612d49e7f29531fe56580b19115a19f98ee3</originalsourceid><addsrcrecordid>eNqFkE1Lw0AQhhdRsFavngNeFEy7n0n3KMFPCh6q52WzmaVb8lGzaTUHwZ_gb_SXuLVFj15mmOF5Z-BB6JTgEcGYjhfG-BHFRGLMGd9DA0okjRPB5T4aYIxlzAVLDtGR94sNQoUcoPdZX3dz8M5fRrruXOVM2-ROl2EqfjbNmytCj7Tp3Np1fdTYKHc-8qvSNrWuXAFjo9tcV7qDqIDWrXUgwe_Ar4_Pcx5KIOtmOYe6Ly-iCrq5ruEYHVhdejjZ9SF6vrl-yu7i6ePtfXY1jQ0TnMfEQMomNi0YIdiYFFhuiSDaGFnkCaEFl5BaKgUjFkQiJjgnkhChibRyAsCG6Gx7d9k2LyvwnVo0q7YOLxXllHImUiYDNdpSQYH3LVi1bF2l214RrDaK1Uax-lUcAnIbeHUl9P_Q6iHLZn_Zb9UOhDc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2422435739</pqid></control><display><type>article</type><title>Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane</title><source>Wiley Journals</source><creator>Nagalakshmamma, Vadabingi ; Varalakshmi, Mavallur ; Umapriya, Kollu ; Venkataswamy, Mallepogu ; Venkataramaiah, Chintha ; Thyaga Raju, Kedam ; Chalapathi, Ponne Venkata ; NagaRaju, Chamarthi</creator><creatorcontrib>Nagalakshmamma, Vadabingi ; Varalakshmi, Mavallur ; Umapriya, Kollu ; Venkataswamy, Mallepogu ; Venkataramaiah, Chintha ; Thyaga Raju, Kedam ; Chalapathi, Ponne Venkata ; NagaRaju, Chamarthi</creatorcontrib><description>A series of new bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl)methane 3(a–d)/5(a–f) were synthesized from bis‐(4‐aminophenyl)methane (1) using various pharmacologically active sulfonyl chlorides 2(a–d) and carbonochloridates 4(a–f) in high yields. The structures of all the newly synthesized compounds were characterized by the Infrared spectroscopy, NMR (1H and 13C), mass, and elemental analyses. Further, all the synthesized compounds were tested for the antioxidant activity by using 2, 2‐diphenyl‐1‐picrylhydrazyl, NO, and H2O2 scavenging methods and antimicrobial activity. Most of the compounds exhibited good antioxidant and antimicrobial activities.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.201900434</identifier><language>eng</language><publisher>Weinheim: Wiley‐VCH Verlag GmbH &amp; Co. KGaA</publisher><subject>Antiinfectives and antibacterials ; antimicrobial activity ; Antimicrobial agents ; antioxidant activity ; Antioxidants ; bis‐(4‐aminophenyl) methane ; carbonyl chloridates ; Derivatives ; Hydrogen peroxide ; Infrared analysis ; Methane ; NMR ; Nuclear magnetic resonance ; Scavenging ; Sulfonamides ; sulfonyl chlorides ; Synthesis</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2020-07, Vol.67 (7), p.1289-1295</ispartof><rights>2020 The Chemical Society Located in Taipei &amp; Wiley‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3544-1ce738f7d3110cc7e3bf151acc9db612d49e7f29531fe56580b19115a19f98ee3</citedby><cites>FETCH-LOGICAL-c3544-1ce738f7d3110cc7e3bf151acc9db612d49e7f29531fe56580b19115a19f98ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjccs.201900434$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjccs.201900434$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Nagalakshmamma, Vadabingi</creatorcontrib><creatorcontrib>Varalakshmi, Mavallur</creatorcontrib><creatorcontrib>Umapriya, Kollu</creatorcontrib><creatorcontrib>Venkataswamy, Mallepogu</creatorcontrib><creatorcontrib>Venkataramaiah, Chintha</creatorcontrib><creatorcontrib>Thyaga Raju, Kedam</creatorcontrib><creatorcontrib>Chalapathi, Ponne Venkata</creatorcontrib><creatorcontrib>NagaRaju, Chamarthi</creatorcontrib><title>Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane</title><title>Journal of the Chinese Chemical Society (Taipei)</title><description>A series of new bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl)methane 3(a–d)/5(a–f) were synthesized from bis‐(4‐aminophenyl)methane (1) using various pharmacologically active sulfonyl chlorides 2(a–d) and carbonochloridates 4(a–f) in high yields. The structures of all the newly synthesized compounds were characterized by the Infrared spectroscopy, NMR (1H and 13C), mass, and elemental analyses. Further, all the synthesized compounds were tested for the antioxidant activity by using 2, 2‐diphenyl‐1‐picrylhydrazyl, NO, and H2O2 scavenging methods and antimicrobial activity. Most of the compounds exhibited good antioxidant and antimicrobial activities.</description><subject>Antiinfectives and antibacterials</subject><subject>antimicrobial activity</subject><subject>Antimicrobial agents</subject><subject>antioxidant activity</subject><subject>Antioxidants</subject><subject>bis‐(4‐aminophenyl) methane</subject><subject>carbonyl chloridates</subject><subject>Derivatives</subject><subject>Hydrogen peroxide</subject><subject>Infrared analysis</subject><subject>Methane</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Scavenging</subject><subject>Sulfonamides</subject><subject>sulfonyl chlorides</subject><subject>Synthesis</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkE1Lw0AQhhdRsFavngNeFEy7n0n3KMFPCh6q52WzmaVb8lGzaTUHwZ_gb_SXuLVFj15mmOF5Z-BB6JTgEcGYjhfG-BHFRGLMGd9DA0okjRPB5T4aYIxlzAVLDtGR94sNQoUcoPdZX3dz8M5fRrruXOVM2-ROl2EqfjbNmytCj7Tp3Np1fdTYKHc-8qvSNrWuXAFjo9tcV7qDqIDWrXUgwe_Ar4_Pcx5KIOtmOYe6Ly-iCrq5ruEYHVhdejjZ9SF6vrl-yu7i6ePtfXY1jQ0TnMfEQMomNi0YIdiYFFhuiSDaGFnkCaEFl5BaKgUjFkQiJjgnkhChibRyAsCG6Gx7d9k2LyvwnVo0q7YOLxXllHImUiYDNdpSQYH3LVi1bF2l214RrDaK1Uax-lUcAnIbeHUl9P_Q6iHLZn_Zb9UOhDc</recordid><startdate>202007</startdate><enddate>202007</enddate><creator>Nagalakshmamma, Vadabingi</creator><creator>Varalakshmi, Mavallur</creator><creator>Umapriya, Kollu</creator><creator>Venkataswamy, Mallepogu</creator><creator>Venkataramaiah, Chintha</creator><creator>Thyaga Raju, Kedam</creator><creator>Chalapathi, Ponne Venkata</creator><creator>NagaRaju, Chamarthi</creator><general>Wiley‐VCH Verlag GmbH &amp; Co. KGaA</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>202007</creationdate><title>Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane</title><author>Nagalakshmamma, Vadabingi ; Varalakshmi, Mavallur ; Umapriya, Kollu ; Venkataswamy, Mallepogu ; Venkataramaiah, Chintha ; Thyaga Raju, Kedam ; Chalapathi, Ponne Venkata ; NagaRaju, Chamarthi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3544-1ce738f7d3110cc7e3bf151acc9db612d49e7f29531fe56580b19115a19f98ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Antiinfectives and antibacterials</topic><topic>antimicrobial activity</topic><topic>Antimicrobial agents</topic><topic>antioxidant activity</topic><topic>Antioxidants</topic><topic>bis‐(4‐aminophenyl) methane</topic><topic>carbonyl chloridates</topic><topic>Derivatives</topic><topic>Hydrogen peroxide</topic><topic>Infrared analysis</topic><topic>Methane</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Scavenging</topic><topic>Sulfonamides</topic><topic>sulfonyl chlorides</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagalakshmamma, Vadabingi</creatorcontrib><creatorcontrib>Varalakshmi, Mavallur</creatorcontrib><creatorcontrib>Umapriya, Kollu</creatorcontrib><creatorcontrib>Venkataswamy, Mallepogu</creatorcontrib><creatorcontrib>Venkataramaiah, Chintha</creatorcontrib><creatorcontrib>Thyaga Raju, Kedam</creatorcontrib><creatorcontrib>Chalapathi, Ponne Venkata</creatorcontrib><creatorcontrib>NagaRaju, Chamarthi</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagalakshmamma, Vadabingi</au><au>Varalakshmi, Mavallur</au><au>Umapriya, Kollu</au><au>Venkataswamy, Mallepogu</au><au>Venkataramaiah, Chintha</au><au>Thyaga Raju, Kedam</au><au>Chalapathi, Ponne Venkata</au><au>NagaRaju, Chamarthi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><date>2020-07</date><risdate>2020</risdate><volume>67</volume><issue>7</issue><spage>1289</spage><epage>1295</epage><pages>1289-1295</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>A series of new bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl)methane 3(a–d)/5(a–f) were synthesized from bis‐(4‐aminophenyl)methane (1) using various pharmacologically active sulfonyl chlorides 2(a–d) and carbonochloridates 4(a–f) in high yields. The structures of all the newly synthesized compounds were characterized by the Infrared spectroscopy, NMR (1H and 13C), mass, and elemental analyses. Further, all the synthesized compounds were tested for the antioxidant activity by using 2, 2‐diphenyl‐1‐picrylhydrazyl, NO, and H2O2 scavenging methods and antimicrobial activity. Most of the compounds exhibited good antioxidant and antimicrobial activities.</abstract><cop>Weinheim</cop><pub>Wiley‐VCH Verlag GmbH &amp; Co. KGaA</pub><doi>10.1002/jccs.201900434</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0009-4536
ispartof Journal of the Chinese Chemical Society (Taipei), 2020-07, Vol.67 (7), p.1289-1295
issn 0009-4536
2192-6549
language eng
recordid cdi_proquest_journals_2422435739
source Wiley Journals
subjects Antiinfectives and antibacterials
antimicrobial activity
Antimicrobial agents
antioxidant activity
Antioxidants
bis‐(4‐aminophenyl) methane
carbonyl chloridates
Derivatives
Hydrogen peroxide
Infrared analysis
Methane
NMR
Nuclear magnetic resonance
Scavenging
Sulfonamides
sulfonyl chlorides
Synthesis
title Synthesis, antimicrobial and antioxidant activity of bis sulfonamide/carbamate derivatives of bis‐(4‐aminophenyl) methane
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T13%3A21%3A12IST&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,%20antimicrobial%20and%20antioxidant%20activity%20of%20bis%20sulfonamide/carbamate%20derivatives%20of%20bis%E2%80%90(4%E2%80%90aminophenyl)%20methane&rft.jtitle=Journal%20of%20the%20Chinese%20Chemical%20Society%20(Taipei)&rft.au=Nagalakshmamma,%20Vadabingi&rft.date=2020-07&rft.volume=67&rft.issue=7&rft.spage=1289&rft.epage=1295&rft.pages=1289-1295&rft.issn=0009-4536&rft.eissn=2192-6549&rft_id=info:doi/10.1002/jccs.201900434&rft_dat=%3Cproquest_cross%3E2422435739%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=2422435739&rft_id=info:pmid/&rfr_iscdi=true