Loading…
Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides
Various novel barbituric and thiobarbituric acid derived sulphonamides were synthesized in excellent yield via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. The compounds 1‐7 were found to exhibit a low to moderate acti...
Saved in:
Published in: | Journal of the Chinese Chemical Society (Taipei) 2011-08, Vol.58 (4), p.528-537 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93 |
---|---|
cites | cdi_FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93 |
container_end_page | 537 |
container_issue | 4 |
container_start_page | 528 |
container_title | Journal of the Chinese Chemical Society (Taipei) |
container_volume | 58 |
creator | Rauf, A. Ahmed, F. Qureshi, A. M. Aziz-ur-Rehman Khan, A. Qadir, M. I. Choudhary, M. I. Chohan, Z. H. Youssoufid, M. H. Haddad, T. Ben |
description | Various novel barbituric and thiobarbituric acid derived sulphonamides were synthesized in excellent yield via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. The compounds 1‐7 were found to exhibit a low to moderate activity whereas compounds 8‐14 showed a significant activity (88.3‐99.9% inhibition determined at 500 μM concentration). Structures of the synthesized compounds were confirmed by 1H‐NMR, 13C‐NMR, mass spectrometry and elemental analysis data.
It reports the synthesis of novel barbituric and thiobarbituric acid derived sulphonamides via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. |
doi_str_mv | 10.1002/jccs.201190017 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jccs_201190017</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JCCS201190017</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93</originalsourceid><addsrcrecordid>eNqFkEFPwjAYhhujiYhePfcPDNt13egRp04I0cNAvDVd-y0rwkbaTeXfC2LQm6cveb_3eQ8PQteUDCgh4c1Saz8ICaWCEJqcoF5IRRjEPBKnqEcIEUHEWXyOLrxfEhKxkIse0vm2bivw1mNVGzx3oDzgcV3Zwra2qXHedsaCx02Jb5XbhZ2z-rs7q2xT_EYjbQ2-A2ffweC8W22qplZra8BforNSrTxc_dw-mj_cz9LHYPqcjdPRNNAsTpKA0SJODAMxBKaMLghQnpS8YMAEjQwJSxoVjIMqqYZ4GIm4gGj3IdyESoFgfTQ47GrXeO-glBtn18ptJSVyr0juFcmjoh0gDsCHXcH2n7acpGn-lw0OrPUtfB5Z5d5knLCEy8VTJrOX7HWyWFAp2BetXHvx</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Rauf, A. ; Ahmed, F. ; Qureshi, A. M. ; Aziz-ur-Rehman ; Khan, A. ; Qadir, M. I. ; Choudhary, M. I. ; Chohan, Z. H. ; Youssoufid, M. H. ; Haddad, T. Ben</creator><creatorcontrib>Rauf, A. ; Ahmed, F. ; Qureshi, A. M. ; Aziz-ur-Rehman ; Khan, A. ; Qadir, M. I. ; Choudhary, M. I. ; Chohan, Z. H. ; Youssoufid, M. H. ; Haddad, T. Ben</creatorcontrib><description>Various novel barbituric and thiobarbituric acid derived sulphonamides were synthesized in excellent yield via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. The compounds 1‐7 were found to exhibit a low to moderate activity whereas compounds 8‐14 showed a significant activity (88.3‐99.9% inhibition determined at 500 μM concentration). Structures of the synthesized compounds were confirmed by 1H‐NMR, 13C‐NMR, mass spectrometry and elemental analysis data.
It reports the synthesis of novel barbituric and thiobarbituric acid derived sulphonamides via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease.</description><identifier>ISSN: 0009-4536</identifier><identifier>EISSN: 2192-6549</identifier><identifier>DOI: 10.1002/jccs.201190017</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Antiurease ; Barbituric and thiobarbituric acids based sulphonamides</subject><ispartof>Journal of the Chinese Chemical Society (Taipei), 2011-08, Vol.58 (4), p.528-537</ispartof><rights>Copyright © 2011 The Chemical Society Located in Taipei & Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim, Germany</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93</citedby><cites>FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Rauf, A.</creatorcontrib><creatorcontrib>Ahmed, F.</creatorcontrib><creatorcontrib>Qureshi, A. M.</creatorcontrib><creatorcontrib>Aziz-ur-Rehman</creatorcontrib><creatorcontrib>Khan, A.</creatorcontrib><creatorcontrib>Qadir, M. I.</creatorcontrib><creatorcontrib>Choudhary, M. I.</creatorcontrib><creatorcontrib>Chohan, Z. H.</creatorcontrib><creatorcontrib>Youssoufid, M. H.</creatorcontrib><creatorcontrib>Haddad, T. Ben</creatorcontrib><title>Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides</title><title>Journal of the Chinese Chemical Society (Taipei)</title><addtitle>Jnl Chinese Chemical Soc</addtitle><description>Various novel barbituric and thiobarbituric acid derived sulphonamides were synthesized in excellent yield via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. The compounds 1‐7 were found to exhibit a low to moderate activity whereas compounds 8‐14 showed a significant activity (88.3‐99.9% inhibition determined at 500 μM concentration). Structures of the synthesized compounds were confirmed by 1H‐NMR, 13C‐NMR, mass spectrometry and elemental analysis data.
It reports the synthesis of novel barbituric and thiobarbituric acid derived sulphonamides via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease.</description><subject>Antiurease</subject><subject>Barbituric and thiobarbituric acids based sulphonamides</subject><issn>0009-4536</issn><issn>2192-6549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkEFPwjAYhhujiYhePfcPDNt13egRp04I0cNAvDVd-y0rwkbaTeXfC2LQm6cveb_3eQ8PQteUDCgh4c1Saz8ICaWCEJqcoF5IRRjEPBKnqEcIEUHEWXyOLrxfEhKxkIse0vm2bivw1mNVGzx3oDzgcV3Zwra2qXHedsaCx02Jb5XbhZ2z-rs7q2xT_EYjbQ2-A2ffweC8W22qplZra8BforNSrTxc_dw-mj_cz9LHYPqcjdPRNNAsTpKA0SJODAMxBKaMLghQnpS8YMAEjQwJSxoVjIMqqYZ4GIm4gGj3IdyESoFgfTQ47GrXeO-glBtn18ptJSVyr0juFcmjoh0gDsCHXcH2n7acpGn-lw0OrPUtfB5Z5d5knLCEy8VTJrOX7HWyWFAp2BetXHvx</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Rauf, A.</creator><creator>Ahmed, F.</creator><creator>Qureshi, A. M.</creator><creator>Aziz-ur-Rehman</creator><creator>Khan, A.</creator><creator>Qadir, M. I.</creator><creator>Choudhary, M. I.</creator><creator>Chohan, Z. H.</creator><creator>Youssoufid, M. H.</creator><creator>Haddad, T. Ben</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201108</creationdate><title>Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides</title><author>Rauf, A. ; Ahmed, F. ; Qureshi, A. M. ; Aziz-ur-Rehman ; Khan, A. ; Qadir, M. I. ; Choudhary, M. I. ; Chohan, Z. H. ; Youssoufid, M. H. ; Haddad, T. Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Antiurease</topic><topic>Barbituric and thiobarbituric acids based sulphonamides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rauf, A.</creatorcontrib><creatorcontrib>Ahmed, F.</creatorcontrib><creatorcontrib>Qureshi, A. M.</creatorcontrib><creatorcontrib>Aziz-ur-Rehman</creatorcontrib><creatorcontrib>Khan, A.</creatorcontrib><creatorcontrib>Qadir, M. I.</creatorcontrib><creatorcontrib>Choudhary, M. I.</creatorcontrib><creatorcontrib>Chohan, Z. H.</creatorcontrib><creatorcontrib>Youssoufid, M. H.</creatorcontrib><creatorcontrib>Haddad, T. Ben</creatorcontrib><collection>Istex</collection><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>Rauf, A.</au><au>Ahmed, F.</au><au>Qureshi, A. M.</au><au>Aziz-ur-Rehman</au><au>Khan, A.</au><au>Qadir, M. I.</au><au>Choudhary, M. I.</au><au>Chohan, Z. H.</au><au>Youssoufid, M. H.</au><au>Haddad, T. Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides</atitle><jtitle>Journal of the Chinese Chemical Society (Taipei)</jtitle><addtitle>Jnl Chinese Chemical Soc</addtitle><date>2011-08</date><risdate>2011</risdate><volume>58</volume><issue>4</issue><spage>528</spage><epage>537</epage><pages>528-537</pages><issn>0009-4536</issn><eissn>2192-6549</eissn><abstract>Various novel barbituric and thiobarbituric acid derived sulphonamides were synthesized in excellent yield via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease. The compounds 1‐7 were found to exhibit a low to moderate activity whereas compounds 8‐14 showed a significant activity (88.3‐99.9% inhibition determined at 500 μM concentration). Structures of the synthesized compounds were confirmed by 1H‐NMR, 13C‐NMR, mass spectrometry and elemental analysis data.
It reports the synthesis of novel barbituric and thiobarbituric acid derived sulphonamides via three components single pot reaction; and these were screened for in vitro urease inhibition studies against jack bean urease.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/jccs.201190017</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-4536 |
ispartof | Journal of the Chinese Chemical Society (Taipei), 2011-08, Vol.58 (4), p.528-537 |
issn | 0009-4536 2192-6549 |
language | eng |
recordid | cdi_crossref_primary_10_1002_jccs_201190017 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Antiurease Barbituric and thiobarbituric acids based sulphonamides |
title | Synthesis and Urease Inhibition Studies of Barbituric and Thiobarbituric Acid Derived Sulphonamides |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T03%3A07%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20Urease%20Inhibition%20Studies%20of%20Barbituric%20and%20Thiobarbituric%20Acid%20Derived%20Sulphonamides&rft.jtitle=Journal%20of%20the%20Chinese%20Chemical%20Society%20(Taipei)&rft.au=Rauf,%20A.&rft.date=2011-08&rft.volume=58&rft.issue=4&rft.spage=528&rft.epage=537&rft.pages=528-537&rft.issn=0009-4536&rft.eissn=2192-6549&rft_id=info:doi/10.1002/jccs.201190017&rft_dat=%3Cwiley_cross%3EJCCS201190017%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3677-31b67d3e98e3adcb0e157f5b3e3914d02f14b35eaf1ce68496be491405d2aae93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |