Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents
The aim of the research work was to synthesize different biologically active carbamate derivatives bearing 2-furoyl-1piperazine and having modest toxicity. The synthesis was completed as a multiple sequence. The structural confirmation of all the synthesized compounds was obtained by EI-MS, IR and 1...
Published in: | Acta Chimica Slovenica |
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Language: | English |
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Slovensko Kemijsko Drustvo
2017
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Online Access: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016141011&doi=10.17344%2facsi.2016.2986&partnerID=40&md5=7140d305b8ff7e5b37003272919cb91a |
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2-s2.0-85016141011 Abbasi M.A.; Hussain G.; Aziz-Ur-Rehman; Siddiqui S.Z.; Ali Shah S.A.; Lodhi M.A.; Ali Khan F.; Ashraf M.; Qurat-Ul-Ain; Ahmad I.; Malik R.; Shahid M.; Mushtaq Z. Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents 2017 Acta Chimica Slovenica 64 1 10.17344/acsi.2016.2986 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016141011&doi=10.17344%2facsi.2016.2986&partnerID=40&md5=7140d305b8ff7e5b37003272919cb91a The aim of the research work was to synthesize different biologically active carbamate derivatives bearing 2-furoyl-1piperazine and having modest toxicity. The synthesis was completed as a multiple sequence. The structural confirmation of all the synthesized compounds was obtained by EI-MS, IR and 1H-NMR spectral data. The enzyme inhibition and antibacterial potential of the synthesized compounds was evaluated. To find the utility of the prepared compounds as possible therapeutic agents their cytotoxicity was also checked. All the compounds were active against acetylcholinesterase enzyme, especially 12 and 14 showed very good inhibitory potential relative to Eserine, a reference standard. Almost all the compounds showed good activities against both Gram-positive and Gram-negative bacterial strains. Slovensko Kemijsko Drustvo 13180207 English Article All Open Access; Gold Open Access |
author |
Abbasi M.A.; Hussain G.; Aziz-Ur-Rehman; Siddiqui S.Z.; Ali Shah S.A.; Lodhi M.A.; Ali Khan F.; Ashraf M.; Qurat-Ul-Ain; Ahmad I.; Malik R.; Shahid M.; Mushtaq Z. |
spellingShingle |
Abbasi M.A.; Hussain G.; Aziz-Ur-Rehman; Siddiqui S.Z.; Ali Shah S.A.; Lodhi M.A.; Ali Khan F.; Ashraf M.; Qurat-Ul-Ain; Ahmad I.; Malik R.; Shahid M.; Mushtaq Z. Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
author_facet |
Abbasi M.A.; Hussain G.; Aziz-Ur-Rehman; Siddiqui S.Z.; Ali Shah S.A.; Lodhi M.A.; Ali Khan F.; Ashraf M.; Qurat-Ul-Ain; Ahmad I.; Malik R.; Shahid M.; Mushtaq Z. |
author_sort |
Abbasi M.A.; Hussain G.; Aziz-Ur-Rehman; Siddiqui S.Z.; Ali Shah S.A.; Lodhi M.A.; Ali Khan F.; Ashraf M.; Qurat-Ul-Ain; Ahmad I.; Malik R.; Shahid M.; Mushtaq Z. |
title |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
title_short |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
title_full |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
title_fullStr |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
title_full_unstemmed |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
title_sort |
Synthesis of some unique carbamate derivatives bearing 2-furoyl-1-piperazine as a valuable therapeutic agents |
publishDate |
2017 |
container_title |
Acta Chimica Slovenica |
container_volume |
64 |
container_issue |
1 |
doi_str_mv |
10.17344/acsi.2016.2986 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016141011&doi=10.17344%2facsi.2016.2986&partnerID=40&md5=7140d305b8ff7e5b37003272919cb91a |
description |
The aim of the research work was to synthesize different biologically active carbamate derivatives bearing 2-furoyl-1piperazine and having modest toxicity. The synthesis was completed as a multiple sequence. The structural confirmation of all the synthesized compounds was obtained by EI-MS, IR and 1H-NMR spectral data. The enzyme inhibition and antibacterial potential of the synthesized compounds was evaluated. To find the utility of the prepared compounds as possible therapeutic agents their cytotoxicity was also checked. All the compounds were active against acetylcholinesterase enzyme, especially 12 and 14 showed very good inhibitory potential relative to Eserine, a reference standard. Almost all the compounds showed good activities against both Gram-positive and Gram-negative bacterial strains. |
publisher |
Slovensko Kemijsko Drustvo |
issn |
13180207 |
language |
English |
format |
Article |
accesstype |
All Open Access; Gold Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678484839071744 |